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Paola S. Dal Cin, Ph.D.

TitleProfessor of Pathology
InstitutionBrigham and Women's Hospital
DepartmentPathology
AddressBrigham and Women's Hospital
Pathology, CAMD, Shapiro5-058
75 Francis St
Boston MA 02115
Phone8573071524
Fax8573071522

 Bibliographic 
 selected publications
Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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  1. Schwind S, Edwards CG, Nicolet D, Mrózek K, Maharry K, Wu YZ, Paschka P, Eisfeld AK, Hoellerbauer P, Becker H, Metzeler KH, Curfman J, Kohlschmidt J, Prior TW, Kolitz JE, Blum W, Pettenati MJ, Dal Cin P, Carroll AJ, Caligiuri MA, Larson RA, Volinia S, Marcucci G, Bloomfield CD. inv(16)/t(16;16) acute myeloid leukemia with non-type A CBFB-MYH11 fusions associate with distinct clinical and genetic features and lack KIT mutations. Blood. 2013 Jan 10; 121(2):385-91.
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  2. Lee CH, Ali RH, Rouzbahman M, Marino-Enriquez A, Zhu M, Guo X, Brunner AL, Chiang S, Leung S, Nelnyk N, Huntsman DG, Blake Gilks C, Nielsen TO, Dal Cin P, van de Rijn M, Oliva E, Fletcher JA, Nucci MR. Cyclin D1 as a diagnostic immunomarker for endometrial stromal sarcoma with YWHAE-FAM22 rearrangement. Am J Surg Pathol. 2012 Oct; 36(10):1562-70.
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  3. Doyle LA, Wang WL, Dal Cin P, Lopez-Terrada D, Mertens F, Lazar AJ, Fletcher CD, Hornick JL. MUC4 is a sensitive and extremely useful marker for sclerosing epithelioid fibrosarcoma: association with FUS gene rearrangement. Am J Surg Pathol. 2012 Oct; 36(10):1444-51.
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  4. Sioletic S, Dal Cin P, Fletcher CD, Hornick JL. Well-differentiated and dedifferentiated liposarcomas with prominent myxoid stroma: analysis of 56 cases. Histopathology. 2013 Jan; 62(2):287-93.
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  5. Brown JR, Hanna M, Tesar B, Werner L, Pochet N, Asara JM, Wang YE, Dal Cin P, Fernandes SM, Thompson C, Macconaill L, Wu CJ, Van de Peer Y, Correll M, Regev A, Neuberg D, Freedman AS. Integrative genomic analysis implicates gain of PIK3CA at 3q26 and MYC at 8q24 in chronic lymphocytic leukemia. Clin Cancer Res. 2012 Jul 15; 18(14):3791-802.
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  6. Lee CH, Mariño-Enriquez A, Ou W, Zhu M, Ali RH, Chiang S, Amant F, Gilks CB, van de Rijn M, Oliva E, Debiec-Rychter M, Dal Cin P, Fletcher JA, Nucci MR. The clinicopathologic features of YWHAE-FAM22 endometrial stromal sarcomas: a histologically high-grade and clinically aggressive tumor. Am J Surg Pathol. 2012 May; 36(5):641-53.
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  7. Kluk MJ, Chapuy B, Sinha P, Roy A, Dal Cin P, Neuberg DS, Monti S, Pinkus GS, Shipp MA, Rodig SJ. Immunohistochemical detection of MYC-driven diffuse large B-cell lymphomas. PLoS One. 2012; 7(4):e33813.
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  8. Dal Cin P, McLaughlin C. Metaphase harvest and cytogenetic analysis of malignant hematological specimens. Curr Protoc Hum Genet. 2012 Apr; Chapter 10:Unit10.2.
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  9. Lee CH, Ou WB, Mariño-Enriquez A, Zhu M, Mayeda M, Wang Y, Guo X, Brunner AL, Amant F, French CA, West RB, McAlpine JN, Gilks CB, Yaffe MB, Prentice LM, McPherson A, Jones SJ, Marra MA, Shah SP, van de Rijn M, Huntsman DG, Dal Cin P, Debiec-Rychter M, Nucci MR, Fletcher JA. 14-3-3 fusion oncogenes in high-grade endometrial stromal sarcoma. Proc Natl Acad Sci U S A. 2012 Jan 17; 109(3):929-34.
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  10. Qian X, Hornick JL, Cibas ES, Dal Cin P, Domanski HA. Angiomatoid fibrous histiocytoma a series of five cytologic cases with literature review and emphasis on diagnostic pitfalls. Diagn Cytopathol. 2012 Aug; 40 Suppl 2:E86-93.
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  11. Wang L, Motoi T, Khanin R, Olshen A, Mertens F, Bridge J, Dal Cin P, Antonescu CR, Singer S, Hameed M, Bovee JV, Hogendoorn PC, Socci N, Ladanyi M. Identification of a novel, recurrent HEY1-NCOA2 fusion in mesenchymal chondrosarcoma based on a genome-wide screen of exon-level expression data. Genes Chromosomes Cancer. 2012 Feb; 51(2):127-39.
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  12. Mosquera JM, Dal Cin P, Mertz KD, Perner S, Davis IJ, Fisher DE, Rubin MA, Hirsch MS. Validation of a TFE3 break-apart FISH assay for Xp11.2 translocation renal cell carcinomas. Diagn Mol Pathol. 2011 Sep; 20(3):129-37.
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  13. Carette JE, Raaben M, Wong AC, Herbert AS, Obernosterer G, Mulherkar N, Kuehne AI, Kranzusch PJ, Griffin AM, Ruthel G, Dal Cin P, Dye JM, Whelan SP, Chandran K, Brummelkamp TR. Ebola virus entry requires the cholesterol transporter Niemann-Pick C1. Nature. 2011 Sep 15; 477(7364):340-3.
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  14. Armand P, Kim HT, Zhang MJ, Perez WS, Dal Cin PS, Klumpp TR, Waller EK, Litzow MR, Liesveld JL, Lazarus HM, Artz AS, Gupta V, Savani BN, McCarthy PL, Cahn JY, Schouten HC, Finke J, Ball ED, Aljurf MD, Cutler CS, Rowe JM, Antin JH, Isola LM, Di Bartolomeo P, Camitta BM, Miller AM, Cairo MS, Stockerl-Goldstein K, Sierra J, Savoie ML, Halter J, Stiff PJ, Nabhan C, Jakubowski AA, Bunjes DW, Petersdorf EW, Devine SM, Maziarz RT, Bornhauser M, Lewis VA, Marks DI, Bredeson CN, Soiffer RJ, Weisdorf DJ. Classifying cytogenetics in patients with acute myelogenous leukemia in complete remission undergoing allogeneic transplantation: a Center for International Blood and Marrow Transplant Research study. Biol Blood Marrow Transplant. 2012 Feb; 18(2):280-8.
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  15. Ligon AH, Morton CC, Bieber FR, Fletcher JA, Giersch AB, Kantarci S, Leach N, Lee C, Sandstrom M, Weremowicz S, Xiao S, Dal Cin P. Reporting of diagnostic cytogenetic results. Curr Protoc Hum Genet. 2011 Jul; Appendix 1:1D.
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  16. Antonescu CR, Zhang L, Nielsen GP, Rosenberg AE, Dal Cin P, Fletcher CD. Consistent t(1;10) with rearrangements of TGFBR3 and MGEA5 in both myxoinflammatory fibroblastic sarcoma and hemosiderotic fibrolipomatous tumor. Genes Chromosomes Cancer. 2011 Oct; 50(10):757-64.
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  17. Gibson SE, Swerdlow SH, Ferry JA, Surti U, Dal Cin P, Harris NL, Hasserjian RP. Reassessment of small lymphocytic lymphoma in the era of monoclonal B-cell lymphocytosis. Haematologica. 2011 Aug; 96(8):1144-52.
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  18. Hasserjian RP, Dal Cin P. Deletion of chromosome 20q: friend or foe? Leuk Res. 2011 Jul; 35(7):844-5.
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  19. Doyle LA, Möller E, Dal Cin P, Fletcher CD, Mertens F, Hornick JL. MUC4 is a highly sensitive and specific marker for low-grade fibromyxoid sarcoma. Am J Surg Pathol. 2011 May; 35(5):733-41.
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  20. Leon A, Staropoli JF, Hernandez JM, Longtine JA, Kuo FC, Dal Cin P. Translocation t(1;9) is a recurrent cytogenetic abnormality associated with progression of essential thrombocythemia patients displaying the JAK2 V617F mutation. Leuk Res. 2011 Sep; 35(9):1188-92.
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  21. McDonald AG, Dal Cin P, Ganguly A, Campbell S, Imai Y, Rosenberg AE, Oliva E. Liposarcoma arising in uterine lipoleiomyoma: a report of 3 cases and review of the literature. Am J Surg Pathol. 2011 Feb; 35(2):221-7.
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  22. Poitras JL, Costa D, Kluk MJ, Amrein PC, Stone RM, Lee C, Dal Cin P, Morton CC. Genomic alterations in myeloid neoplasms with novel, apparently balanced translocations. Cancer Genet. 2011 Feb; 204(2):68-76.
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  23. Liang CW, Mariño-Enríquez A, Johannessen C, Hornick JL, Dal Cin P. Translocation (Y;12) in lipoma. Cancer Genet. 2011 Jan; 204(1):53-6.
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  24. Ordulu Z, Dal Cin P, Chong WW, Choy KW, Lee C, Muto MG, Quade BJ, Morton CC. Disseminated peritoneal leiomyomatosis after laparoscopic supracervical hysterectomy with characteristic molecular cytogenetic findings of uterine leiomyoma. Genes Chromosomes Cancer. 2010 Dec; 49(12):1152-60.
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  25. Smoley SA, Van Dyke DL, Kay NE, Heerema NA, Dell' Aquila ML, Dal Cin P, Koduru P, Aviram A, Rassenti L, Byrd JC, Rai KR, Brown JR, Greaves AW, Eckel-Passow J, Neuberg D, Kipps TJ, Dewald GW. Standardization of fluorescence in situ hybridization studies on chronic lymphocytic leukemia (CLL) blood and marrow cells by the CLL Research Consortium. Cancer Genet Cytogenet. 2010 Dec; 203(2):141-8.
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  26. Antonescu CR, Zhang L, Chang NE, Pawel BR, Travis W, Katabi N, Edelman M, Rosenberg AE, Nielsen GP, Dal Cin P, Fletcher CD. EWSR1-POU5F1 fusion in soft tissue myoepithelial tumors. A molecular analysis of sixty-six cases, including soft tissue, bone, and visceral lesions, showing common involvement of the EWSR1 gene. Genes Chromosomes Cancer. 2010 Dec; 49(12):1114-24.
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  27. Heerema NA, Byrd JC, Dal Cin PS, Dell' Aquila ML, Koduru PR, Aviram A, Smoley SA, Rassenti LZ, Greaves AW, Brown JR, Rai KR, Kipps TJ, Kay NE, Van Dyke DL. Stimulation of chronic lymphocytic leukemia cells with CpG oligodeoxynucleotide gives consistent karyotypic results among laboratories: a CLL Research Consortium (CRC) Study. Cancer Genet Cytogenet. 2010 Dec; 203(2):134-40.
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  28. Sandberg AA, Meloni-Ehrig AM, Van den Berghe H, Dal Cin P, Block AW. Editorial communication. Cancer Genet Cytogenet. 2010 Dec; 203(2):101.
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  29. Roper N, DeAngelo DJ, Kuo F, Dal Cin P, Ghobrial I, Aster JC. An asymptomatic 61-year-old man with BCR-ABL-positive bone marrow following autologous transplantation for multiple myeloma. Am J Hematol. 2010 Dec; 85(12):944-6.
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  30. Choueiri TK, Lim ZD, Hirsch MS, Tamboli P, Jonasch E, McDermott DF, Dal Cin P, Corn P, Vaishampayan U, Heng DY, Tannir NM. Vascular endothelial growth factor-targeted therapy for the treatment of adult metastatic Xp11.2 translocation renal cell carcinoma. Cancer. 2010 Nov 15; 116(22):5219-25.
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  31. Elco CP, Mariño-Enríquez A, Abraham JA, Dal Cin P, Hornick JL. Hybrid myxoinflammatory fibroblastic sarcoma/hemosiderotic fibrolipomatous tumor: report of a case providing further evidence for a pathogenetic link. Am J Surg Pathol. 2010 Nov; 34(11):1723-7.
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  32. Butrynski JE, D'Adamo DR, Hornick JL, Dal Cin P, Antonescu CR, Jhanwar SC, Ladanyi M, Capelletti M, Rodig SJ, Ramaiya N, Kwak EL, Clark JW, Wilner KD, Christensen JG, Jänne PA, Maki RG, Demetri GD, Shapiro GI. Crizotinib in ALK-rearranged inflammatory myofibroblastic tumor. N Engl J Med. 2010 Oct 28; 363(18):1727-33.
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  33. Ligon AH, Morton CC, Bieber FR, Fletcher JA, Giersch AB, Kantarci S, Leach N, Lee C, Sandstrom M, Weremowicz S, Xiao S, Dal Cin P. Reporting of diagnostic cytogenetic results. Curr Protoc Hum Genet. 2010 Oct; Appendix 1:1D.1-23.
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  34. Huang D, Sumegi J, Dal Cin P, Reith JD, Yasuda T, Nelson M, Muirhead D, Bridge JA. C11orf95-MKL2 is the resulting fusion oncogene of t(11;16)(q13;p13) in chondroid lipoma. Genes Chromosomes Cancer. 2010 Sep; 49(9):810-8.
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  35. Romeo S, Duim RA, Bridge JA, Mertens F, de Jong D, Dal Cin P, Wijers-Koster PM, Debiec-Rychter M, Sciot R, Rosenberg AE, Szuhai K, Hogendoorn PC. Heterogeneous and complex rearrangements of chromosome arm 6q in chondromyxoid fibroma: delineation of breakpoints and analysis of candidate target genes. Am J Pathol. 2010 Sep; 177(3):1365-76.
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  36. Mariño-Enríquez A, Fletcher CD, Dal Cin P, Hornick JL. Dedifferentiated liposarcoma with "homologous" lipoblastic (pleomorphic liposarcoma-like) differentiation: clinicopathologic and molecular analysis of a series suggesting revised diagnostic criteria. Am J Surg Pathol. 2010 Aug; 34(8):1122-31.
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  37. Medeiros F, Araujo AR, Erickson-Johnson MR, Kashyap PC, Dal Cin P, Nucci M, Wang X, Bell DA, Oliveira AM. HMGA1 and HMGA2 rearrangements in mass-forming endometriosis. Genes Chromosomes Cancer. 2010 Jul; 49(7):630-4.
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  38. Roh MH, Dal Cin P, Silverman SG, Cibas ES. The application of cytogenetics and fluorescence in situ hybridization to fine-needle aspiration in the diagnosis and subclassification of renal neoplasms. Cancer Cytopathol. 2010 Jun 25; 118(3):137-45.
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  39. Kelly PJ, Weiss SE, Sher DJ, Perez-Atayde AR, Dal Cin P, Choueiri TK. Sunitinib-induced pseudoprogression after whole-brain radiotherapy for metastatic renal cell carcinoma. J Clin Oncol. 2010 Sep 1; 28(25):e433-5.
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  40. Guardiola MT, Dobin SM, Dal Cin P, Donner LR. Pericentric inversion (12)(p12q13-14) as the sole chromosomal abnormality in a leiomyoma of the vulva. Cancer Genet Cytogenet. 2010 May; 199(1):21-3.
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  41. Sumegi J, Streblow R, Frayer RW, Dal Cin P, Rosenberg A, Meloni-Ehrig A, Bridge JA. Recurrent t(2;2) and t(2;8) translocations in rhabdomyosarcoma without the canonical PAX-FOXO1 fuse PAX3 to members of the nuclear receptor transcriptional coactivator family. Genes Chromosomes Cancer. 2010 Mar; 49(3):224-36.
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  42. Snuderl M, Kolman OK, Chen YB, Hsu JJ, Ackerman AM, Dal Cin P, Ferry JA, Harris NL, Hasserjian RP, Zukerberg LR, Abramson JS, Hochberg EP, Lee H, Lee AI, Toomey CE, Sohani AR. B-cell lymphomas with concurrent IGH-BCL2 and MYC rearrangements are aggressive neoplasms with clinical and pathologic features distinct from Burkitt lymphoma and diffuse large B-cell lymphoma. Am J Surg Pathol. 2010 Mar; 34(3):327-40.
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  43. Dal Cin P, Aster JC, DeAngelo DJ. When to go FISHing. Am J Clin Pathol. 2010 Mar; 133(3):351-3.
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  44. Chou RC, Dinarello CA, Ferry JA, Dal Cin P. A 36-year-old woman with recurrent high-grade fevers, hypotension, and hypertriglyceridemia. Arthritis Care Res (Hoboken). 2010 Jan 15; 62(1):128-36.
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  45. Yoda A, Yoda Y, Chiaretti S, Bar-Natan M, Mani K, Rodig SJ, West N, Xiao Y, Brown JR, Mitsiades C, Sattler M, Kutok JL, DeAngelo DJ, Wadleigh M, Piciocchi A, Dal Cin P, Bradner JE, Griffin JD, Anderson KC, Stone RM, Ritz J, Foà R, Aster JC, Frank DA, Weinstock DM. Functional screening identifies CRLF2 in precursor B-cell acute lymphoblastic leukemia. Proc Natl Acad Sci U S A. 2010 Jan 5; 107(1):252-7.
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  46. Factor RE, Dal Cin P, Fletcher JA, Cibas ES. Cytogenetics and fluorescence in situ hybridization as adjuncts to cytology in the diagnosis of malignant mesothelioma. Cancer. 2009 Aug 25; 117(4):247-53.
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  47. Snyder EL, Sandstrom DJ, Law K, Fiore C, Sicinska E, Brito J, Bailey D, Fletcher JA, Loda M, Rodig SJ, Dal Cin P, Fletcher CD. c-Jun amplification and overexpression are oncogenic in liposarcoma but not always sufficient to inhibit the adipocytic differentiation programme. J Pathol. 2009 Jul; 218(3):292-300.
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  48. Staropoli JF, Wadleigh M, Dal Cin P. Derivative (1)t(1;19)(p13;p13) in the setting of myelofibrosis with JAK2 V617F. Cancer Genet Cytogenet. 2009 Jun; 191(2):109-10.
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  49. Hornick JL, Dal Cin P, Fletcher CD. Loss of INI1 expression is characteristic of both conventional and proximal-type epithelioid sarcoma. Am J Surg Pathol. 2009 Apr; 33(4):542-50.
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  50. Brown JR, Friedberg JW, Feng Y, Scofield S, Phillips K, Dal Cin P, Joyce R, Takvorian RW, Fisher DC, Fisher RI, Liesveld J, Marquis D, Neuberg D, Freedman AS. A phase 2 study of concurrent fludarabine and rituximab for the treatment of marginal zone lymphomas. Br J Haematol. 2009 Jun; 145(6):741-8.
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  51. Soupir CP, Vergilio JA, Kelly E, Dal Cin P, Kuter D, Hasserjian RP. Identification of del(20q) in a subset of patients diagnosed with idiopathic thrombocytopenic purpura. Br J Haematol. 2009 Mar; 144(5):800-2.
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  52. Poitras JL, Dal Cin P, Aster JC, Deangelo DJ, Morton CC. Novel SSBP2-JAK2 fusion gene resulting from a t(5;9)(q14.1;p24.1) in pre-B acute lymphocytic leukemia. Genes Chromosomes Cancer. 2008 Oct; 47(10):884-9.
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  53. Mertz KD, Demichelis F, Sboner A, Hirsch MS, Dal Cin P, Struckmann K, Storz M, Scherrer S, Schmid DM, Strebel RT, Probst-Hensch NM, Gerstein M, Moch H, Rubin MA. Association of cytokeratin 7 and 19 expression with genomic stability and favorable prognosis in clear cell renal cell cancer. Int J Cancer. 2008 Aug 1; 123(3):569-76.
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  54. Wang WL, Mayordomo E, Czerniak BA, Abruzzo LV, Dal Cin P, Araujo DM, Lev DC, López-Terrada D, Lazar AJ. Fluorescence in situ hybridization is a useful ancillary diagnostic tool for extraskeletal myxoid chondrosarcoma. Mod Pathol. 2008 Nov; 21(11):1303-10.
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  55. Hodge JC, Quade BJ, Rubin MA, Stewart EA, Dal Cin P, Morton CC. Molecular and cytogenetic characterization of plexiform leiomyomata provide further evidence for genetic heterogeneity underlying uterine fibroids. Am J Pathol. 2008 May; 172(5):1403-10.
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  56. Palacios Calvo J, Dal Cin P. Uterine cancer: Screening, Diagnosis, and Treatment. Current clinical Oncology. Muggia F, Olivia E. 2008.
  57. Dal Cin P, Ligon A. Urinary Tract. Cancer Cytogenetics, Third Edition. Heim S, Mitelman F. 2008.
  58. Antonescu CR, Dal Cin P, Nafa K, Teot LA, Surti U, Fletcher CD, Ladanyi M. EWSR1-CREB1 is the predominant gene fusion in angiomatoid fibrous histiocytoma. Genes Chromosomes Cancer. 2007 Dec; 46(12):1051-60.
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  59. Han M, Rivera MN, Batten JM, Haber DA, Dal Cin P, Iafrate AJ. Wilms' tumor with an apparently balanced translocation t(X;18) resulting in deletion of the WTX gene. Genes Chromosomes Cancer. 2007 Oct; 46(10):909-13.
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  60. Deng J, Carlson N, Takeyama K, Dal Cin P, Shipp M, Letai A. BH3 profiling identifies three distinct classes of apoptotic blocks to predict response to ABT-737 and conventional chemotherapeutic agents. Cancer Cell. 2007 Aug; 12(2):171-85.
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  61. Takeyama K, Monti S, Manis JP, Dal Cin P, Getz G, Beroukhim R, Dutt S, Aster JC, Alt FW, Golub TR, Shipp MA. Integrative analysis reveals 53BP1 copy loss and decreased expression in a subset of human diffuse large B-cell lymphomas. Oncogene. 2008 Jan 10; 27(3):318-22.
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  62. McCluggage WG, Sumathi VP, Nucci MR, Hirsch M, Dal Cin P, Wells M, Flanagan AM, Fisher C. Ewing family of tumours involving the vulva and vagina: report of a series of four cases. J Clin Pathol. 2007 Jun; 60(6):674-80.
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  63. Nucci MR, Drapkin R, Dal Cin P, Fletcher CD, Fletcher JA. Distinctive cytogenetic profile in benign metastasizing leiomyoma: pathogenetic implications. Am J Surg Pathol. 2007 May; 31(5):737-43.
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  64. Soupir CP, Vergilio JA, Dal Cin P, Muzikansky A, Kantarjian H, Jones D, Hasserjian RP. Philadelphia chromosome-positive acute myeloid leukemia: a rare aggressive leukemia with clinicopathologic features distinct from chronic myeloid leukemia in myeloid blast crisis. Am J Clin Pathol. 2007 Apr; 127(4):642-50.
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  65. Hornick JL Dal Cin P, Fletcher CDM. Loss of INI1 Expression Is Characteristic of Both Conventional And Proximal-Type Epithelioid Sarcoma. United States and Canadian Academy of Pathology. 2007; San Diego, California .
  66. Antonescu CR, Dal Cin P, Nafa K, Teot LA, CFletcher CD, Ladanyi M. EWS-CREB1 is the Predominant Gene Fusion in Angiomatoid Fibrous Histiocytoma. United States and Canadian Academy of Pathology. 2007; San Diego, California.
  67. Bossuyt V , Ginevan K, Dal Cin P, Fletcher J, Cibas E S. . The value of cytogenetics as an adjunct to cytology in the diagnosis of non-hematopoietic neoplasms. United States and Canadian Academy of Pathology. 2007; San Diego, California .
  68. Dal Cin P, Yee AJ, Dey B. . A de novo AML with a t(1;21)(p36;q22) in an elderly patient. Atlas Genet Cytogenet Oncol Haematol. 2007.
  69. Dal Cin, Ouahchi K. t(16;21)(q24;q22) in therapy-related acute myelogenous leukemia arising from myelodysplastic syndromeAtlas Genet Cytogenet Oncol Haematol. 2007.
  70. Lindeman N, Dal Cin P. . Molecular testing for solid tumors. Essential of Molecular Genetic Pathology.Cheng L, Zhang D. eds. 2007.
  71. Ladany M, Antonescu C, Dal Cin P. Molecular genetics and cytogenetics analysis of soft tissue tumors. Enzinger &Weiss Soft Tissue Tumors 5th Ed. Weiss SW, Goldblum JR eds. 2007.
  72. Nucci MR, Harburger D, Koontz J, Dal Cin P, Sklar J. Molecular analysis of the JAZF1-JJAZ1 gene fusion by RT-PCR and fluorescence in situ hybridization in endometrial stromal neoplasms. Am J Surg Pathol. 2007 Jan; 31(1):65-70.
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  73. Durkin S, Ligon A, Kelly A, McLaughlin C, Dal Cin P. . Fishing for solutions: Adjust FISH analysis for myeloid malignancies with a non-clonal abnormality identified cytogenetically. 32nd AGT Annual Meeting. 2007; Denver, Colorado.
  74. Rassenti, LZ, Huynh L, Basak GW, Ghia E, van Dyke D, Heerema N, Zahrein D, Dal Cin P, Dell'Aquila ML, Doduru P, Byrd JC, kay NE, Rai KR, Brown JR, Wierda WG, Greaves AW, Croce Cm, Kippis TJ. . TCL1 Expersssion in Chronic Lymphocytic Lukemia corrolares with the intensity of 11q Deletions and ZAP-70. The American Society of Hematology. 2007.
  75. Roehrl MH, Selig MK, Nielsen GP, Dal Cin P, Oliva E. A renal cell carcinoma with components of both chromophobe and papillary carcinoma. Virchows Arch. 2007 Jan; 450(1):93-101.
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  76. Rodig SJ, Healey BM, Pinkus GS, Kuo FC, Dal Cin P, Kutok JL. Mantle cell lymphoma arising within primary nodal marginal zone lymphoma: a unique presentation of two uncommon B-cell lymphoproliferative disorders. Cancer Genet Cytogenet. 2006 Nov; 171(1):44-51.
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  77. Rabban JT, Dal Cin P, Oliva E. HMGA2 rearrangement in a case of vulvar aggressive angiomyxoma. Int J Gynecol Pathol. 2006 Oct; 25(4):403-7.
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  78. Antonescu CR, Nafa K, Segal NH, Dal Cin P, Ladanyi M. EWS-CREB1: a recurrent variant fusion in clear cell sarcoma--association with gastrointestinal location and absence of melanocytic differentiation. Clin Cancer Res. 2006 Sep 15; 12(18):5356-62.
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  79. Takahashi H, Feuerhake F, Kutok JL, Monti S, Dal Cin P, Neuberg D, Aster JC, Shipp MA. FAS death domain deletions and cellular FADD-like interleukin 1beta converting enzyme inhibitory protein (long) overexpression: alternative mechanisms for deregulating the extrinsic apoptotic pathway in diffuse large B-cell lymphoma subtypes. Clin Cancer Res. 2006 Jun 1; 12(11 Pt 1):3265-71.
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  80. Hirsch MS, Dal Cin P, Fletcher CD. ALK expression in pseudosarcomatous myofibroblastic proliferations of the genitourinary tract. Histopathology. 2006 Apr; 48(5):569-78.
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  81. Christacos NC, Quade BJ, Dal Cin P, Morton CC. Uterine leiomyomata with deletions of Ip represent a distinct cytogenetic subgroup associated with unusual histologic features. Genes Chromosomes Cancer. 2006 Mar; 45(3):304-12.
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  82. Antonescu CR, K Nafa K, Dal Cin P , Ladanyi M. EWS-CREB1: A recurrent variant fusion in clear cell sarcoma associated with gastrointestinal location and absence of melanocytic differentiation. United States and Canadian Academy of Pathology. 2006; Atlanta, Georgia.
  83. Durkin S, Ligon A, McLaughlin C, Dal Cin P. Clinical Cytogenetic Analysis of Lymph Node Speciments. 2006.
  84. Moore SD, Offor O, Ferry JA, Amrein PC, Morton CC, Dal Cin P. ELF4 is fused to ERG in a case of acute myeloid leukemia with a t(X;21)(q25-26;q22). Leuk Res. 2006 Aug; 30(8):1037-42.
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  85. Ligon AH, DeAngelo DJ, Atkins L, Dal Cin P. Isochromosome of a deleted 20q may be a relatively common abnormality in myeloid malignancies. Cancer Genet Cytogenet. 2005 Oct 1; 162(1):89-91.
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  86. Srivastava A, Nielsen PG, Dal Cin P, Rosenberg AE. Monophasic synovial sarcoma of the liver. Arch Pathol Lab Med. 2005 Aug; 129(8):1047-9.
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  87. Christacos NC, Sherman L, Roy A, DeAngelo DJ, Dal Cin P. Is the cryptic interstitial deletion of 8q24 surrounding MYC a common mechanism in the formation of double minute chromosome? Cancer Genet Cytogenet. 2005 Aug; 161(1):90-2.
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  88. Oliveira AM, Perez-Atayde AR, Dal Cin P, Gebhardt MC, Chen CJ, Neff JR, Demetri GD, Rosenberg AE, Bridge JA, Fletcher JA. Aneurysmal bone cyst variant translocations upregulate USP6 transcription by promoter swapping with the ZNF9, COL1A1, TRAP150, and OMD genes. Oncogene. 2005 May 12; 24(21):3419-26.
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  89. Oliveira AM, Perez-Atayde AR, Dal Cin P, Gebhardt MC, Rosenberg RE, Bridge JA, and Fletcher JA . Novel USP6 Tfusion omcogenes with TRAP150, ZNF9, Osteomodulin and COL1A1 in aneurysmal bone cyst variant translocations. United States and Canadian Academy of Pathology. 2005; San Antonio, Texas.
  90. Moore SD, Strehl S, Dal Cin P. Acute myelocytic leukemia with t(11;17)(q23;q12-q21) involves a fusion of MLL and AF17. Cancer Genet Cytogenet. 2005 Feb; 157(1):87-9.
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  91. Dal Cin P, Morton CC . Cytogenetic and Other Genetic Insights into the Pathogenesis of Uterine Leiomyomata. Uterine Leiomyomata: Pathogenesis and Management. 2005.
  92. Monti S, Savage KJ, Kutok JL, Feuerhake F, Kurtin P, Mihm M, Bingyan Wu B, Pasqualucci L, Neuberg D, Aguiar RCT, Dal Cin P, Ladd C, Pinkus GS, Salles G, Harris NL, Dalla-Favera R, Habermann TM, Aster JC, Golub TR, Shipp MA. Molecular profiling of diffuse large B-cell lymphoma reveals discrete cluster including one characterized by host inflammatory response. American Society of Hematology, 47th Annual Meeting. 2004; San Diego, CA.
  93. Wang L, Pitman MB, Castillo CF, Dal Cin P, Oliva E. Choriocarcinoma involving the pancreas as first manifestation of a metastatic regressing mixed testicular germ cell tumor. Mod Pathol. 2004 Dec; 17(12):1573-80.
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  94. Monti S, Savage KJ, Kutok JL, Feuerhake F, Kurtin P, Mihm M, Wu B, Pasqualucci L, Neuberg D, Aguiar RC, Dal Cin P, Ladd C, Pinkus GS, Salles G, Harris NL, Dalla-Favera R, Habermann TM, Aster JC, Golub TR, Shipp MA. Molecular profiling of diffuse large B-cell lymphoma identifies robust subtypes including one characterized by host inflammatory response. Blood. 2005 Mar 1; 105(5):1851-61.
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  95. Ligon AH, Morton CC, Bieber FR, Fletcher JA, Giersch AB, Lee C, Sandstrom M, Weremowicz S, Xiao S, Dal Cin P. Reporting of diagnostic cytogenetic results. Curr Protoc Hum Genet. 2004 Nov; Appendix 1:Appendix 1D.
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  96. Moore SDP, Dal Cin P, Quade BJ, Herrick SR, Ince T, Parisi M, Mealiffe M, Harris DJ, Ferguson HL, Strehl S, Ligon AH, Kleinman M, Kucherlapati R, Morton CC. Tumor Genome Anatomy Project (TGAP): Gene discovery in tumors in the genome era. American Society of Human Genetics. 52th Annual Meeting. 2004; Toronto, Canada.
  97. Moore SD, Herrick SR, Ince TA, Kleinman MS, Dal Cin P, Morton CC, Quade BJ. Uterine leiomyomata with t(10;17) disrupt the histone acetyltransferase MORF. Cancer Res. 2004 Aug 15; 64(16):5570-7.
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  98. Nascimento AF, Dal Cin P, Cilento BG, Perez-Atayde AR, Kozakewich HP, Nosé V. Urachal inflammatory myofibroblastic tumor with ALK gene rearrangement: a study of urachal remnants. Urology. 2004 Jul; 64(1):140-4.
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  99. Ferguson B. Dubois Z, Merkhofer E, McLaughlin C, Powell K, Roy A, Sherman L, Soltisova D, Dal Cin P. A technical approach to cytogenetic and molecular investigation of chronic lymphocytic leukemia. Association of Genetic Technologists, 29th Annual Meeting. 2004; Anaheim, CA.
  100. Roy A, Sandstrom D, Dal Cin P. . Clinical importance of fluorescence in situ hybridization in hematologic disorders. Association of Genetic Technologists, 29th Annual Meeting. 2004; Anaheim, CA.
  101. Quade BJ, Wang TY, Sornberger K, Dal Cin P, Mutter GL, Morton CC. Molecular pathogenesis of uterine smooth muscle tumors from transcriptional profiling. Genes Chromosomes Cancer. 2004 Jun; 40(2):97-108.
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  102. Joniau S, Goeman L, Kreuzbauer S, Bogaert G, Dal Cin P, Oyen R, Sciot R, van Poppel H. Benign renal mesenchymoma in the pediatric age group: a novel pathologic and karyotype entity. Urology. 2004 May; 63(5):981-4.
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  103. Oliveira AM, Hsi BL, Weremowicz S, Rosenberg AE, Dal Cin P, Joseph N, Bridge JA, Perez-Atayde AR, Fletcher JA. USP6 (Tre2) fusion oncogenes in aneurysmal bone cyst. Cancer Res. 2004 Mar 15; 64(6):1920-3.
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  104. Moore SDP, Herrick SR, Ince T, Dal Cin P, Kleinman M, Morton CC, Quade BJ. Chromosome 10 rearrarangements in uterine leiomyomata involve the histone acetyltransferase MORF. United States and Canadian Academy of Pathology. 2004; Vancouver, Can.
  105. Oliveira AM, Hsi B-L, Weromowicz S, Perez-Ayade AR, Rosenberg AE, Dal Cin P, Joseph N, Bridge JA, Fletcher JA. Translocation (16;17)(q22;p13) fuses osteobalstic cadherin CDH11 to USP6 in aneurysmal bone cysts. United States and Canadian Academy of Pathology. 2004; Vancouver, Canada.
  106. Dal Cin P, Thomas A, Weremowicz S. An intragenic rearrangement of HMGA2 is not necessary for lipoma formation. Cancer Genet Cytogenet. 2004 Mar; 149(2):178-9.
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  107. Dal Cin P, Sherman L, Marzelli M, McLaughlin C, Zukerberg L, Amrein PC. A new case of t(11;17)(q23;q21) with MLL rearrangement. Cancer Genet Cytogenet. 2004 Jan 15; 148(2):178-9.
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  108. Ligon AH, Morton CC, Bieber FR, Fletcher JA, Giersch AB, Lee C, Sandstrom M, Weremowicz S, Xiao S, Dal Cin P. Reporting of Diagnostic Cytogenetic Results. Current Protocols in Human Genetics. Drapoli NC, Haines JL, Korf BR, Morton CC, Seidman CE, Seidman JG, Smith DR, eds. 2004; Supplement 43:A.1D.1 - A1D.27.
  109. Si MW,Thorson JA, Lauwers GY, Dal Cin P, Furman J. Hepatocellular lymphoepithelioma-like carcinoma associated with Epstein Barr Virus: a hitherto unrecognized entity. Diagnostic Mol Pathol. 2004; 13:183-9.
  110. Savage KJ, Monti S, Kutok JL, Cattoretti G, Neuberg D, de Laval L, Kurtin P, Dal Cin P, Ladd C, Feuerhake F, Aguiar R, Li S, Salles G, Berger F, Jing W, Pinkus G, Habermann T, Dalla-Favera R, Harris N, Aster JC, Golub T, Shipp M. The molecular signature of mediastinal large B-cell lymphoma differs from that of other diffuse Large B-cell lymphomas and shares features with classical Hodgkin’s lymphoma. American Society of Hematology, 45th Annual Meeting. 2003; San Diego, CA.
  111. Feuerhake F, Dal Cin P, Kurtin P, Pasqualucci L, Savage KJ, Kutok JL, Neuberg D , Aguiar RC, Monti S, Ladd C, Cattoretti G, Pinkus GS, Harris NL, Habermann T,Golub TR, Dalla-Favera R, Aster JC, Shipp MA. Genetic heterogeneity in diffuse large B-cell lymphoma (DLBCL): Chromosomal translocations and increased copy numbers, gene amplification, and aberrant somatic hypermutation. American Society of Hematology, 45th Annual Meeting. 2003; San Diego, CA.
  112. Drandi D, Lee C, Dal Cin P, Gribben JG. Array-based comparative genomic hybridization identifies deletion at 14q32 as a new prognostic marker in chronic lymphocytic leukemia (CLL). American Society of Hematology, 45th Annual Meeting. 2003; San Diego, CA.
  113. Moore SDP, Herrick SR, Ince T, Dal Cin P, Klienman M Morton CC, Quade BJ. Cytogenetic chararacterization of uterine leiomyoma with t(10;17) involve the histone acetyltransferase MORF. American Society of Human Genetics. 52th Annual Meeting. 2003; Los Angeles, CA.
  114. Christacos N, Dal Cin P, Morton CC, Quade BJ. Cellular leiomyoma: a genetically distinct entity among benign uterine tumors. American Society of Human Genetics. 52th Annual Meeting. 2003; Los Angeles, CA.
  115. Lee C, Drandi SD, Dal Cin P, Gribben JG. Prognostic marker in CLL by array-based comparative genomic hyndidization. American Society of Human Genetics. 52th Annual Meeting. 2003; Los Angeles, CA.
  116. Dal Cin P. Genetics in renal cell carcinoma. Curr Opin Urol. 2003 Nov; 13(6):463-6.
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  117. Pentimalli F, Dentice M, Fedele M, Pierantoni GM, Cito L, Pallante P, Santoro M, Viglietto G, Dal Cin P, Fusco A. Suppression of HMGA2 protein synthesis could be a tool for the therapy of well differentiated liposarcomas overexpressing HMGA2. Cancer Res. 2003 Nov 1; 63(21):7423-7.
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  118. Drandi D, Lee C, Dal Cin P, Gribben JG. Array-based comparative Genomic Hybridization: A new molecular technology to study genomic imbalances in CLL. 39th Congresso Nazionale della Societa’ Italiana di Ematologia. 2003; Roma, Italy.
  119. Drandi D, Lee C, Dal Cin P, Gribben JG. Array-based comparative Genomic Hybridization: Whole Genome Screening in CLL. International Workshop in CLL. 2003; Stresa, Italy.
  120. Duensing S, Lee BH, Dal Cin P, Münger K. Excessive centrosome abnormalities without ongoing numerical chromosome instability in a Burkitt's lymphoma. Mol Cancer. 2003 Sep 8; 2:30.
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  121. Savage KJ, Monti S, Kutok JL, Cattoretti G, Neuberg D, De Leval L, Kurtin P, Dal Cin P, Ladd C, Feuerhake F, Aguiar RC, Li S, Salles G, Berger F, Jing W, Pinkus GS, Habermann T, Dalla-Favera R, Harris NL, Aster JC, Golub TR, Shipp MA. The molecular signature of mediastinal large B-cell lymphoma differs from that of other diffuse large B-cell lymphomas and shares features with classical Hodgkin lymphoma. Blood. 2003 Dec 1; 102(12):3871-9.
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  122. Dal Cin P . . Intravenous leiomyomatosis. Atlas Genet Cytogenet Oncol Haematol. 2003.
  123. Soltisova D, Merkhofer E, Fergusun B, DuBois Z, McLaughlin C, Sherman L, Dal Cin P. Unrelated chromosome abnormalities in hematological malignacies. Association of Genetic Technologists, 28th Annual Meeting. 2003; Atlanta, Georgia.
  124. Drandi D, Lee C, Dal Cin P, Gribben JG. . Comparative genomic hybridization array analysis: A new moecular cytogenetic method to study genomic imbalnce in B-CLL. European conference of the ESF Programme in Functional Genomics. 2003; Prague, Czech Republic.
  125. Varnholt H, Vauthey JN, Dal Cin P, Marsh Rde W, Bhathal PS, Hughes NR, Lauwers GY. Biliary adenofibroma: a rare neoplasm of bile duct origin with an indolent behavior. Am J Surg Pathol. 2003 May; 27(5):693-8.
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  126. Dal Cin P. Metaphase harvest and cytogenetic analysis of malignant hematological specimens. Curr Protoc Hum Genet. 2003 May; Chapter 10:Unit 10.2.
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  127. Dal Cin P, Christacos N, Morton CC, Quade BJ. . Cellular leiomyoma: a genetically distinct entity among benign uterine tumors. United States and Canadian Academy of Pathology. 2003; Washington, DC.
  128. Nucci, MR,Koontz J, Pauwels P, Harbuger D, Dal Cin P, Sklar J. . Assessment of the frequency of t(7;17) in endometrial stromal neoplasia by RT-PCR and FISH. United States and Canadian Academy of Pathology. 2003; Washington, DC.
  129. Hirsh MS, Dal Cin P, Fletcher CDM. ALK expression in reactive pseudosarcomatous myofibroblastic proliferationns of the genitourinary tract. United States and Canadian Academy of Pathology. 2003; Washington, DC .
  130. Nucci, MR, Dal Cin P, Drapkin R, Fletcher CDM, Fletcher JA. . So-called benign metastazing leiomyoma: Cytogenetic analysis confirms a distinct clinopathologic entity. United States and Canadian Academy of Pathology. 2003; Washington, DC.
  131. Quade BJ, Weremowicz S, Neskey DM, Vanni R, Ladd C, Dal Cin P, Morton CC. Fusion transcripts involving HMGA2 are not a common molecular mechanism in uterine leiomyomata with rearrangements in 12q15. Cancer Res. 2003 Mar 15; 63(6):1351-8.
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  132. Dal Cin P, Quade BJ, Neskey DM, Kleinman MS, Weremowicz S, Morton CC. Intravenous leiomyomatosis is characterized by a der(14)t(12;14)(q15;q24). Genes Chromosomes Cancer. 2003 Feb; 36(2):205-6.
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  133. Dal Cin P, Morton CC. . Cytogenetics for the Hematologist. Blood: Principles and Practice of Hematology. 2003; 96-122.
  134. Dal Cin P . Soft Tissue Tumors. Atlas Genet Cytogenet Oncol Haematol. January 2003. . Soft Tissue Tumors. Atlas Genet Cytogenet Oncol Haematol. 2003.
  135. Polito P, Dal Cin P, Debiec-Rychter M, Hagemeijer A. Human solid tumors: cytogenetic techniques. Methods Mol Biol. 2003; 220:135-50.
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  136. Polito P, Dal Cin P, Debiec-Rychter M , Hagemeijer A. Human Solid Tumors: Cytogenetics techniques. Methods in Molecular Biology. Cytogenetics: Methods and Protocols.G.J. Swansbury ed. 2003; 220:135-150.
  137. Panagopoulos I, Mertens F, Isaksson M, Domanski HA, Brosjö O, Heim S, Bjerkehagen B, Sciot R, Dal Cin P, Fletcher JA, Fletcher CD, Mandahl N. Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma. Genes Chromosomes Cancer. 2002 Dec; 35(4):340-52.
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  138. Hirsch MS, Weinstein MH, Thomas A, Dal Cin P. Identical karyotypes in synchronous bilateral clear cell renal cell carcinomas. Cancer Genet Cytogenet. 2002 Nov; 139(1):86-7.
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  139. Neskey DM, Dal Cin P, SWeremowicz S, B.J. Quade BJ, C.C. Morton CC. Understanding the Molecular Mechanism of Dysregulated HMGA2 Expression in Uterine Leiomyomata with 12q15 Rearrangements. American Society of Human Genetics. 51th Annual Meeting. 2002; Philadelphia, USA.
  140. Colwell AS, D'Cunha J, Vargas SO, Parker B, Dal Cin P, Maddaus MA. Synovial sarcoma of the pleura: a clinical and pathologic study of three cases. J Thorac Cardiovasc Surg. 2002 Oct; 124(4):828-32.
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  141. Dal Cin P, Morton CC. 1q42 approximately q44 is rarely cytogenetically involved in sporadic uterine leiomyomata. Cancer Genet Cytogenet. 2002 Oct 1; 138(1):92-3.
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  142. Debiec-Rychter M, Roskam T, Van Poppel H, Dal Cin P, Lerut E, Blyweert W, Hagemeijer A. Cytogenetic findings in 292 primary renal cell tumors. 8th European Conference on Cytogenetics and Molecular Genetics of Human Solid Tumors. 2002; Barcelona, Spain .
  143. Debiec-Rychter M, Roskam T, Van Poppel H, Dal Cin P, Lerut E, Blyweert W, Hagemeijer A. Cytogenetic findings in 292 primary renal cell tumors. 8th European Conference on Cytogenetics and Molecular Genetics of Human Solid Tumors. 2002; Barcelona, Spain .
  144. Debiec-Rychter M, Roskam T, Van Poppel H, Dal Cin P, Lerut E, Blyweert W, Hagemeijer A. Cytogenetic findings in 292 primary renal cell tumors. 8th European Conference on Cytogenetics and Molecular Genetics of Human Solid Tumors. 2002; Barcelona, Spain .
  145. Mertens F, Strömberg U, Mandahl N, Dal Cin P, De Wever I, Fletcher CD, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van Den Berghe H, Vanni R, Willén H. Prognostically important chromosomal aberrations in soft tissue sarcomas: a report of the Chromosomes and Morphology (CHAMP) Study Group. Cancer Res. 2002 Jul 15; 62(14):3980-4.
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  146. Sherman L, Ariynayagam S, Christy K, DuBois Z, Marzelli M, McLaughlin C, Soltisova D, Dal Cin P. Cytogenetic and FISH analyses on chronic lymphocytic leukemias. Association of Genetic Technologists, 27th Annual Meeting. 2002; Cincinnati,OH.
  147. Dal Cin P. . HMGIC(HMGA2) in adipose tissue tumors. Third International Workshop ”HMGA protein in cell differentiation and trasformation”. 2002; Napoli,Italy.
  148. Morton CC, Dal Cin P, Neskey DM,S Weremowicz S, B.J. Quade BJ. Are fusion transcripts involving HMGA2 a common molecular mechanism in uterine leiomyomata with trarrangements in 12q15?. Third International Workshop”HMGA protein in cell differentiation and trasformation”. 2002; Napoli,Italy.
  149. Nilsson M, Höglund M, Panagopoulos I, Sciot R, Dal Cin P, Debiec-Rychter M, Mertens F, Mandahl N. Molecular cytogenetic mapping of recurrent chromosomal breakpoints in tenosynovial giant cell tumors. Virchows Arch. 2002 Nov; 441(5):475-80.
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  150. Dal Cin P, Sciot R, Van Poppel H, Balzarini P, Roskams T, Van den Berghe H. Chromosome changes in sarcomatoid renal carcinomas are different from those in renal cell carcinomas. Cancer Genet Cytogenet. 2002 Apr 1; 134(1):38-40.
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  151. Bloomfield CD, Archer KJ, Mrózek K, Lillington DM, Kaneko Y, Head DR, Dal Cin P, Raimondi SC. 11q23 balanced chromosome aberrations in treatment-related myelodysplastic syndromes and acute leukemia: report from an international workshop. Genes Chromosomes Cancer. 2002 Apr; 33(4):362-78.
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  152. Dal-Cin P, Killian S, Koh A, Lessnick SL, Petersen R, Kimonis V. A case of bilateral retinoblastoma with a constitutional unbalanced translocation (6;15)(q27;q11.2). American College of Medical Genetics, Annual Meeting. 2002; New Orleans, LA.
  153. Quade BJ, Dal Cin P, Neskey DM, Weremowicz S, Morton CC. Intravenous leiomyomatosis: molecular and cytogenetic analysis of a case. Mod Pathol. 2002 Mar; 15(3):351-6.
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  154. Gisselsson D, Pålsson E, Höglund M, Domanski H, Mertens F, Pandis N, Sciot R, Dal Cin P, Bridge JA, Mandahl N. Differentially amplified chromosome 12 sequences in low- and high-grade osteosarcoma. Genes Chromosomes Cancer. 2002 Feb; 33(2):133-40.
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  155. Tallini G, Dorfman H, Brys P, Dal Cin P, De Wever I, Fletcher CD, Jonson K, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Samson I, Sciot R, Van den Berghe H, Vanni R, Willén H. Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group. J Pathol. 2002 Feb; 196(2):194-203.
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  156. Dal Cin P. . Metaphase harvest and cytogenetic analysis of malignant hematological specimen. Current Protocols in Human Genetics, Drapoli NC, Haines JL, Korf BR, Morton CC, Seidman CE, Seidman JG, Smith DR, eds. 2002; 10.2.1-10.2.12.
  157. De Coppi P, Bartsch G, Dal Cin P, Yoo JY, Soker S, Atala A. Human fetal stem cell isolation from amniotic fluid. New Engalnd Section AUA. 2002; Boston, MA.
  158. Quade,BJ,Wang T-Y, Dal Cin P, Mutter GL,Morton CC. Transcriptional profiling of uterine smooth muscle tumors: Progress towards new diagnostic markers. United States and Canadian Academy of Pathology. 2002; Chicago, IL.
  159. De Coppi P, Bartsch G,Perin L, Yoo JY, Dal Cin P, , Soker S, Atala A. . Human embronic and fetal stem cell isolation from chorion villi and amniotic fluid. In vitro and In vivo studies. 2nd Symposiuom on therapeutic applications of human stem cells and precursor cells. 2002; Hannover, Germany.
  160. Nascimento AG, Dal Cin P. Plexiform fibrohistiocytic tumour. Fletcher CDM, Unni KK, Mertens F, editors. World Health Organization Classification of TumoursPathology and Genetics of Tumours of Soft Tissue and Bone. 2002; 116-117.
  161. Aubain Somerhausen N, Dal Cin P. Diffuse-type giant tumour. Fletcher CDM, Unni KK, Mertens F, editors. World Health Organization Classification of TumoursPathology and Genetics of Tumours of Soft Tissue and Bone. 2002; 112-114.
  162. Aubain Somerhausen N, Dal Cin P. . Giant cell tumour of tendon sheath. Fletcher CDM, Unni KK, Mertens F, editors. World Health Organization Classification of TumoursPathology and Genetics of Tumours of Soft Tissue and Bone. 2002; 110-111.
  163. Hirsh Ms, Dal Cin P, Joseph N, Thomas, A, Fletcher JA, Weinstein MH. Assesement of unselected renal epithelial tumors: independent evaluation by cytogenetics and histology. United States and Canadian Academy of Pathology. 2002; Chicago, IL.
  164. Adem C, Gisselsson D, Dal Cin P, Nascimento AG. . Interphase cytogenetics analysis of infantile fibrosarcomas and congenital mesoblastic nephromas. United States and Canadian Academy of Pathology. 2002; Chicago, IL.
  165. Dal Cin P. . Bone: Aneurysmal bone cysts. Atlas Genet Cytogenet Oncol Haematol. 2002.
  166. Bloomfield CD Kellie J Archer KJ, Raimondi SC, Harrison CJ, Kaneko Y,Head D, Dal Cin P, a Rowley JD. 2th International Workshop on BCA in Secondary Leukemia (IWBCASL), (Chicago, IL). Among Therapy-Associated Acute Leukemia Or Myelodysplastic Syndrome (t-AL/MDS) With Balanced Cytogenetic Abnormalities (BCA), Those Involving 11q23 Are Associated With Distinctive Prior Therapeutic Exposures And Clinical Features, Including Adverse Outcome. 43rd ASH Annual Meeting. 2001; Orlando, Fl.
  167. Bovée JV, Sciot R, Dal Cin P, Debiec-Rychter M, van Zelderen-Bhola SL, Cornelisse CJ, Hogendoorn PC. Chromosome 9 alterations and trisomy 22 in central chondrosarcoma: a cytogenetic and DNA flow cytometric analysis of chondrosarcoma subtypes. Diagn Mol Pathol. 2001 Dec; 10(4):228-35.
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  168. French CA, Miyoshi I, Aster JC, Kubonishi I, Kroll TG, Dal Cin P, Vargas SO, Perez-Atayde AR, Fletcher JA. BRD4 bromodomain gene rearrangement in aggressive carcinoma with translocation t(15;19). Am J Pathol. 2001 Dec; 159(6):1987-92.
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  169. Adem C, Gisselsson D, Dal Cin P, Nascimento AG. ETV6 rearrangements in patients with infantile fibrosarcomas and congenital mesoblastic nephromas by fluorescence in situ hybridization. Mod Pathol. 2001 Dec; 14(12):1246-51.
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  170. Van Dorpe J, Dal Cin P, Weremowicz S, Van Leuven F, de Wever I, Van den Berghe H, Fletcher CD, Sciot R. Translocation of the HMGI-C ( HMGA2) gene in a benign mesenchymoma (chondrolipoangioma). Virchows Arch. 2002 May; 440(5):485-90.
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  171. Ginevan KB, Fletcher JA, Dal Cin P, Cibas ES. . The value of cytogenetics as an adjunct to diagnostic fine needle aspiration cytology of nonhematopoietic neoplasms. American Society of Cytopathology. 49TH Scientific Annual Meeting. 2001; Kansas City, Missouri.
  172. Rubin BP, Dal Cin P. The genetics of lipomatous tumors. Semin Diagn Pathol. 2001 Nov; 18(4):286-93.
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  173. Gisselsson D, Jonson T, Petersén A, Strömbeck B, Dal Cin P, Höglund M, Mitelman F, Mertens F, Mandahl N. Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors. Proc Natl Acad Sci U S A. 2001 Oct 23; 98(22):12683-8.
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  174. Weinstein MH, Dal Cin P. Genetics of epithelial tumors of the renal parenchyma in adults and renal cell carcinoma in children. Anal Quant Cytol Histol. 2001 Oct; 23(5):362-72.
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  175. Gisselsson D, Hibbard MK, Dal Cin P, Sciot R, Hsi BL, Kozakewich HP, Fletcher JA. PLAG1 alterations in lipoblastoma: involvement in varied mesenchymal cell types and evidence for alternative oncogenic mechanisms. Am J Pathol. 2001 Sep; 159(3):955-62.
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  176. Debiec-Rychter M, Sciot R, Pauwels P, Schoenmakers E, Dal Cin P, Hagemeijer A. Molecular cytogenetic definition of three distinct chromosome arm 14q deletion intervals in gastrointestinal stromal tumors. Genes Chromosomes Cancer. 2001 Sep; 32(1):26-32.
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  177. Vargas SO, French CA, Faul PN, Fletcher JA, Davis IJ, Dal Cin P, Perez-Atayde AR. Upper respiratory tract carcinoma with chromosomal translocation 15;19: evidence for a distinct disease entity of young patients with a rapidly fatal course. Cancer. 2001 Sep 1; 92(5):1195-203.
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  178. Sjöblom T, Shimizu A, O'Brien KP, Pietras K, Dal Cin P, Buchdunger E, Dumanski JP, Ostman A, Heldin CH. Growth inhibition of dermatofibrosarcoma protuberans tumors by the platelet-derived growth factor receptor antagonist STI571 through induction of apoptosis. Cancer Res. 2001 Aug 1; 61(15):5778-83.
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  179. Panagopoulos I, Mertens F, Isaksson M, Limon J, Gustafson P, Skytting B, Akerman M, Sciot R, Dal Cin P, Samson I, Iliszko M, Ryoe J, Dêbiec-Rychter M, Szadowska A, Brosjö O, Larsson O, Rydholm A, Mandahl N. Clinical impact of molecular and cytogenetic findings in synovial sarcoma. Genes Chromosomes Cancer. 2001 Aug; 31(4):362-72.
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  180. Dal Cin P. . Chromophobe renal cell carcinoma. Atlas Genet Cytogenet Oncol Haematol. 2001.
  181. Ladanyi M, Woodruff JM, Scheithauer BW, Bridge JA, Barr FG, Goldblum JR, Fisher C, Perez-Atayde A, Dal Cin P, Fletcher CD, Fletcher JA. Re: O'Sullivan MJ, Kyriakos M, Zhu X, Wick MR, Swanson PE, Dehner LP, Humphrey PA, Pfeifer JD: malignant peripheral nerve sheath tumors with t(X;18). A pathologic and molecular genetic study. Mod pathol 2000;13:1336-46. Mod Pathol. 2001 Jul; 14(7):733-7.
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  182. Fletcher CD, Fletcher JA, Dal Cin P, Ladanyi M, Woodruff JM. Diagnostic gold standard for soft tissue tumours: morphology or molecular genetics? Histopathology. 2001 Jul; 39(1):100-3.
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  183. Koontz JI, Soreng AL, Nucci M, Kuo FC, Pauwels P, van Den Berghe H, Dal Cin P, Fletcher JA, Sklar J. Frequent fusion of the JAZF1 and JJAZ1 genes in endometrial stromal tumors. Proc Natl Acad Sci U S A. 2001 May 22; 98(11):6348-53.
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  184. Dal Cin P, Atkins L, Ford C, Ariyanayagam S, Armstrong SA, George R, Cleary A, Morton CC. Amplification of AML1 in childhood acute lymphoblastic leukemias. Genes Chromosomes Cancer. 2001 Apr; 30(4):407-9.
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  185. Ladanyi M, Lui MY, Antonescu CR, Krause-Boehm A, Meloni-Ehrig A, Argani P, Sorensen PHB, Mertens F, Mandahl N, Van den Berghe H, Sciot R, Dal Cin P, Bridge J. Cloning of the der(17)t(X;17)(p11;q25) of alveolar soft part sarcoma identifies the ASPL/TFE3 gene fusion, a new molecular diagnostic marker. United States and Canadian Academy of Pathology. 2001; Atlanta, Georgia.
  186. Faul PN, French CA, Vargas SO, Dal Cin P, Fletcher JA, Perez-Atayde AR. Larynx as a primary site for t(15;19) carcinoma, a distinct rapidly fatal disease of young patients. United States and Canadian Academy of Pathology. 2001; Atlanta, Georgia.
  187. Ladanyi M, Lui MY, Antonescu CR, Krause-Boehm A, Meindl A, Argani P, Healey JH, Ueda T, Yoshikawa H, Meloni-Ehrig A, Sorensen PH, Mertens F, Mandahl N, van den Berghe H, Sciot R, Dal Cin P, Bridge J. The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25. Oncogene. 2001 Jan 4; 20(1):48-57.
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  188. Gisselsson D, Björk J, Höglund M, Mertens F, Dal Cin P, Akerman M, Mandahl N. Abnormal nuclear shape in solid tumors reflects mitotic instability. Am J Pathol. 2001 Jan; 158(1):199-206.
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  189. Dal Cin P. . Fibrous dysplasia of the bone. Atlas Genet Cytogenet Oncol Haematol. 2001.
  190. De Coppi P, Bartsch G, Dal Cin P, Yoo JY, Soker S, Atala A. Human fetal stem cell isolation from amniotic fluid. American Academy Pediatrics, Section of Urology. 2001; San Francisco CA.
  191. Dal Cin P, Neskey DM, Weremowicz S, Morton CC, Quade BJ. Intravenous Leiomyomatosis: Is There A Genetic Link With Uterine Leiomyoma?. United States and Canadian Academy of Pathology. 2001; Atlanta, Georgia.
  192. Quade BJ, Neskey DM, Nucci MR, Dal Cin P, WangT-Y. Müllerian Adenosarcomas not characterized by marked chromosomal or genomic nstability. United States and Canadian Academy of Pathology. 2001; Atlanta, Georgia.
  193. Sciot R, Dorfman H, Brys P, Dal Cin P, De Wever I, Fletcher CD, Jonson K, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Samson I, Tallini G, Van den Berghe H, Vanni R, Willén H. Cytogenetic-morphologic correlations in aneurysmal bone cyst, giant cell tumor of bone and combined lesions. A report from the CHAMP study group. Mod Pathol. 2000 Nov; 13(11):1206-10.
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  194. Dal Cin P, Sciot R, Brys P, De Wever I, Dorfman H, Fletcher CD, Jonsson K, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Samson I, Tallini G, Van den Berghe H, Vanni R, Willen H. Recurrent chromosome aberrations in fibrous dysplasia of the bone: a report of the CHAMP study group. CHromosomes And MorPhology. Cancer Genet Cytogenet. 2000 Oct 1; 122(1):30-2.
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  195. De Wever I, Dal Cin P, Fletcher CD, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van Den Berghe H, Vanni R, Willén H. Cytogenetic, clinical, and morphologic correlations in 78 cases of fibromatosis: a report from the CHAMP Study Group. CHromosomes And Morphology. Mod Pathol. 2000 Oct; 13(10):1080-5.
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  196. Vanni R, Fletcher CD, Sciot R, Dal Cin P, De Wever I, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Tallini G, Van Den Berghe H, Willén H. Cytogenetic evidence of clonality in cutaneous benign fibrous histiocytomas: a report of the CHAMP study group. Histopathology. 2000 Sep; 37(3):212-7.
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  197. Hibbard MK, Kozakewich HP, Dal Cin P, Sciot R, Tan X, Xiao S, Fletcher JA. PLAG1 fusion oncogenes in lipoblastoma. Cancer Res. 2000 Sep 1; 60(17):4869-72.
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  198. Lawrence B, Perez-Atayde A, Hibbard MK, Rubin BP, Dal Cin P, Pinkus JL, Pinkus GS, Xiao S, Yi ES, Fletcher CD, Fletcher JA. TPM3-ALK and TPM4-ALK oncogenes in inflammatory myofibroblastic tumors. Am J Pathol. 2000 Aug; 157(2):377-84.
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  199. Pauwels P, Sciot R, Croiset F, Rutten H, Van den Berghe H, Dal Cin P. Myofibroblastoma of the breast: genetic link with spindle cell lipoma. J Pathol. 2000 Jul; 191(3):282-5.
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  200. Dal Cin P, Kozakewich HP, Goumnerova L, Mankin HJ, Rosenberg AE, Fletcher JA. Variant translocations involving 16q22 and 17p13 in solid variant and extraosseous forms of aneurysmal bone cyst. Genes Chromosomes Cancer. 2000 Jun; 28(2):233-4.
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  201. Pauwels P, Dal Cin P, Vlasveld LT, Aleva RM, van Erp WF, Jones D. A chromosomal abnormality in hyaline vascular Castleman's disease: evidence for clonal proliferation of dysplastic stromal cells. Am J Surg Pathol. 2000 Jun; 24(6):882-8.
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  202. Gisselsson D, Pettersson L, Höglund M, Heidenblad M, Gorunova L, Wiegant J, Mertens F, Dal Cin P, Mitelman F, Mandahl N. Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity. Proc Natl Acad Sci U S A. 2000 May 9; 97(10):5357-62.
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  203. Dei Tos AP, Doglioni C, Piccinin S, Sciot R, Furlanetto A, Boiocchi M, Dal Cin P, Maestro R, Fletcher CD, Tallini G. Coordinated expression and amplification of the MDM2, CDK4, and HMGI-C genes in atypical lipomatous tumours. J Pathol. 2000 Apr; 190(5):531-6.
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  204. Tallini G, Vanni R, Manfioletti G, Kazmierczak B, Faa G, Pauwels P, Bullerdiek J, Giancotti V, Van Den Berghe H, Dal Cin P. HMGI-C and HMGI(Y) immunoreactivity correlates with cytogenetic abnormalities in lipomas, pulmonary chondroid hamartomas, endometrial polyps, and uterine leiomyomas and is compatible with rearrangement of the HMGI-C and HMGI(Y) genes. Lab Invest. 2000 Mar; 80(3):359-69.
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  205. Kazmierczak B, Dal Cin P, Rogalla P, Van den Berghe H, Bullerdiek J. Regional fine mapping of HMG17 to chromosomal band 1p35. Cancer Genet Cytogenet. 2000 Jan 15; 116(2):164-5.
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  206. Pauwels P, Ambros P, Hattinger C, Lammens M, Dal Cin P, Ribot J, Struyk A, van den Berghe H. Peripheral primitive neuroectodermal tumour of the cervix. Virchows Arch. 2000 Jan; 436(1):68-73.
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  207. Mertens F, Dal Cin P, De Wever I, Fletcher CDM, Mandahl N, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van den Berghe H, Vanni R, Willén H. Cytogenetic characterization of peripheral nerve sheats tumors. A report of the CHAMP group. 8th International Workshop on Chromosomes in Solid Tumors. 2000; Tucson, AZ.
  208. Dal Cin P, Roskams T, De Vos R, Van Poppel H, Balzarini P, Van Den Berghe H. Involvement of chromosomes 1 and 18 in renal cell tumors. Cancer Genet Cytogenet. 2000 Jan 1; 116(1):54-8.
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  209. Mertens F, Dal Cin P, De Wever I, Fletcher CD, Mandahl N, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, van Den Berghe H, Vanni R, Willén H. Cytogenetic characterization of peripheral nerve sheath tumours: a report of the CHAMP study group. J Pathol. 2000 Jan; 190(1):31-8.
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  210. Mandahl N, Fletcher CD, Dal Cin P, De Wever I, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van Den Berghe H, Vanni R, Willén H. Comparative cytogenetic study of spindle cell and pleomorphic leiomyosarcomas of soft tissues: a report from the CHAMP Study Group. Cancer Genet Cytogenet. 2000 Jan 1; 116(1):66-73.
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  211. Van Poppel H, Nilsson S, Algaba F, Bergerheim U, Dal Cin P, Fleming S, Hellsten S, Kirkali Z, Klotz L, Lindblad P, Ljungberg B, Mulders P, Roskams T, Ross RK, Walker C, Wersäll P. Precancerous lesions in the kidney. Scand J Urol Nephrol Suppl. 2000; (205):136-65.
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  212. Dal Cin P, Kozakewich HP, Weremowicz S, Goumnerova L, Mankin HJ , Rosenberg AE, Fletcher JA. . Translocations involving 16q22 and 17p13 are found in all types of aneurysmal bone cysts. 8th International Workshop on Chromosomes in Solid Tumors. 2000; Tucson, AZ.
  213. Gisselsson D, Pettersson L, Höglund M, Hiedenblad M, Gurunova L, Wiegant J, Mertens F, Dal Cin P, Mitelman F, Mandahl N. Chromosomal breakage-fusion-bridge events cause genetic intratumor heretogeneity. 8th International Workshop on Chromosomes in Solid Tumors. 2000; Tucson, AZ.
  214. Mulier S, Stas M, Delabie J, Lateur L, Gysen M, Dal Cin P, Robberecht C, De Wever I. Proliferative myositis in a child. Skeletal Radiol. 1999 Dec; 28(12):703-9.
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  215. Dal Cin P, Quade BJ, Weremowicz S, Morton CC, Pauwels P, Van Den Berghe H. Primary parauterine leiomyoma with a t(6;14) Genes Chromosomes Cancer. 1999 Dec; 26(4):385-6.
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  216. Tejpar S, Nollet F, Li C, Wunder JS, Michils G, dal Cin P, Van Cutsem E, Bapat B, van Roy F, Cassiman JJ, Alman BA. Predominance of beta-catenin mutations and beta-catenin dysregulation in sporadic aggressive fibromatosis (desmoid tumor). Oncogene. 1999 Nov 11; 18(47):6615-20.
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  217. Quade BJ, Getman M, Wang T-Y, Weremowicz S, Dal Cin P, Morton CC. Exploring the dysregulation of HMGIC in uterine leiomyomata with t(12;14). American Society of Human Genetics. 49th Annual Meeting. 1999; San Francisco, CA.
  218. Dal Cin P, Roskams T, Van Poppel H, Balzarini P, Van den Berghe H. Cytogenetic investigation of transitional cell carcinomas of the upper urinary tract. Cancer Genet Cytogenet. 1999 Oct 15; 114(2):117-20.
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  219. Dal Cin P, Van den Berghe H, Pauwels P. Epithelioid sarcoma of the proximal type with complex karyotype including i(8q) Cancer Genet Cytogenet. 1999 Oct 1; 114(1):80-2.
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  220. Tallini G, Dal Cin P. HMGI(Y) and HMGI-C dysregulation: a common occurrence in human tumors. Adv Anat Pathol. 1999 Sep; 6(5):237-46.
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  221. Balzarini P, Tardanico R, Grigolato P, Cunico SC, Cozzoli A, Zanotelli T, Van Den Berghe H, Dal Cin P. Atypical chromosome abnormalities in a renal oncocytoma. Cancer Genet Cytogenet. 1999 Aug; 113(1):103-4.
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  222. Losi L, Buonamici L, Dal Cin P, Giannini C, Dei Tos P, Calbucci F, Eusebi V. [Cytogenetics of tumors of the central nervous system: a case study and review of the literature]. Pathologica. 1999 Aug; 91(4):249-55.
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  223. Kazmierczak B, Dal Cin P, Sciot R, Van den Berghe H, Bullerdiek J. Inflammatory myofibroblastic tumor with HMGIC rearrangement. Cancer Genet Cytogenet. 1999 Jul 15; 112(2):156-60.
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  224. Dal Cin P, Pauwels P, Van Den Berghe H. Solitary fibrous tumour of the pleura with t(4;15)(q13;q26) Histopathology. 1999 Jul; 35(1):94-5.
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  225. Sciot R, Dal Cin P, Hagemeijer A, De Smet L, Van Damme B, Van den Berghe H. Cutaneous sclerosing perineurioma with cryptic NF2 gene deletion. Am J Surg Pathol. 1999 Jul; 23(7):849-53.
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  226. Buonamici L, Roncaroli F, Fioravanti A, Losi L, Van den Berghe H, Calbucci F, Dal Cin P. Cytogenetic investigation of chordomas of the skull. Cancer Genet Cytogenet. 1999 Jul 1; 112(1):49-52.
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  227. Van den Berghe I, Dal Cin P, De Groef K, Michielssen P, Van den Berghe H. Monosomy 22 and trisomy 14 may be early events in the tumorigenesis of adult granulosa cell tumor. Cancer Genet Cytogenet. 1999 Jul 1; 112(1):46-8.
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  228. Gisselsson D, Höglund M, Mertens F, Dal Cin P, Mandahl N. Hibernomas are characterized by homozygous deletions in the multiple endocrine neoplasia type I region. Metaphase fluorescence in situ hybridization reveals complex rearrangements not detected by conventional cytogenetics. Am J Pathol. 1999 Jul; 155(1):61-6.
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  229. Vanni R, Marras S, Faa G, Uccheddu A, Dal Cin P, Sciot R, Samson I, Van den Berghe H. Chromosome instability in elastofibroma. Cancer Genet Cytogenet. 1999 Jun; 111(2):182-3.
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  230. Sciot R, Rosai J, Dal Cin P, de Wever I, Fletcher CD, Mandahl N, Mertens F, Mitelman F, Rydholm A, Tallini G, van den Berghe H, Vanni R, Willén H. Analysis of 35 cases of localized and diffuse tenosynovial giant cell tumor: a report from the Chromosomes and Morphology (CHAMP) study group. Mod Pathol. 1999 Jun; 12(6):576-9.
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  231. Sciot R, Samson I, van den Berghe H, Van Damme B, Dal Cin P. Collagenous fibroma (desmoplastic fibroblastoma): genetic link with fibroma of tendon sheath? Mod Pathol. 1999 Jun; 12(6):565-8.
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  232. Fletcher CD, Dal Cin P, de Wever I, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, van den Berghe H, Vanni R, Willén H. Correlation between clinicopathological features and karyotype in spindle cell sarcomas. A report of 130 cases from the CHAMP study group. Am J Pathol. 1999 Jun; 154(6):1841-7.
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  233. Gisselsson D, Höglund M, Mertens F, Johansson B, Dal Cin P, Van den Berghe H, Earnshaw WC, Mitelman F, Mandahl N. The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells. Hum Genet. 1999 Apr; 104(4):315-25.
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  234. Van den Berghe I, Dal Cin P, Sciot R, Vanvuchelen J, Michielssen P, Hagemeijer A, De Baene L, Van den Berghe H. Translocation (4;8) as a primary chromosome change in a hydropic leiomyoma. Histopathology. 1999 Apr; 34(4):378.
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  235. Losi L, Dal Cin P. [Telomeres: a review of the literature]. Pathologica. 1999 Apr; 91(2):121-3.
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  236. Balzarini P, Grigolato P, Tardanico R, Cadei M, Cunico SC, Cozzoli A, Zanotelli T, van den Berghe H, Dal Cin P. Multitechnical pathological diagnosis in chromophobe renal cell carcinoma. Oncol Rep. 1999 Mar-Apr; 6(2):295-9.
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  237. Dal Cin P, Bertoni F, Bacchini P, Hagemeijer A, Van den Berghe H. Fibrous dysplasia and the short arm of chromosome 12. Histopathology. 1999 Mar; 34(3):279-80.
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  238. Kazmierczak B, Dal Cin P, Meyer-Bolte K, Van den Berghe H, Bullerdiek J. HMG1 is not rearranged by 13q12 aberrations in lipomas. Genes Chromosomes Cancer. 1999 Mar; 24(3):290-2.
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  239. Dal Cin P, Fusco A, Belge G, Chiappetta G, Fedele M, Pauwels P, Bullerdiek J, Van den Berghe H. Involvement of the HMGI(Y) gene in a microfollicular adenoma of the thyroid. Genes Chromosomes Cancer. 1999 Mar; 24(3):286-9.
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  240. Polito P, Dal Cin P, Sciot R, Brock P, Van Eyken P, Van den Berghe H. Embryonal rhabdomyosarcoma with only numerical chromosome changes. Case report and review of the literature. Cancer Genet Cytogenet. 1999 Mar; 109(2):161-5.
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  241. Brosens I, Dal Cin P, Deprest J, Van den Berghe H. Clinico-pathological features of uterine leiomyomas. "Pathogenesis and Medical Management of Uterine Fibroids": Satellite session of the 5th International Symposium on GnRH Analogues in Cancer and Human Reproduction. 1999; Geneva, Switzerland.
  242. Dal Cin P, Pauwels P, Poldermans LJ, Sciot R, Van den Berghe H. Clonal chromosome abnormalities in a so-called Dupuytren's subungual exostosis. Genes Chromosomes Cancer. 1999 Feb; 24(2):162-4.
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  243. Pauwels P, Dal Cin P, Roumen R, van den Berghe H, Sciot R. Intramuscular mixed tumour with clonal chromosomal changes. Virchows Arch. 1999 Feb; 434(2):167-71.
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  244. Sciot R, Dal Cin P, Samson I, van den Berghe H, Van Damme B. Clonal chromosomal changes in juxta-articular myxoma. Virchows Arch. 1999 Feb; 434(2):177-80.
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  245. Polito P, Dal Cin P, Kazmierczak B, Rogalla P, Bullerdiek J, Van den Berghe H. Deletion of HMG17 in uterine leiomyomas with ring chromosome 1. Cancer Genet Cytogenet. 1999 Jan 15; 108(2):107-9.
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  246. Dal Cin P, De Smet L, Sciot R, Van Damme B, Van den Berghe H. Trisomy 7 and trisomy 8 in dividing and non-dividing tumor cells in Dupuytren's disease. Cancer Genet Cytogenet. 1999 Jan 15; 108(2):137-40.
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  247. Pauwels P, Dal Cin P, Sciot R, Lammens M, Penn O, van Nes E, Kwee WS, van den Berghe H. Primary malignant peripheral nerve sheath tumour of the heart. Histopathology. 1999 Jan; 34(1):56-9.
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  248. Brosens I., Dal Cin P., Deprest J., Van den Berghe H. . Clinico-pathological features of uterine leiomyomas. Pathogenesis and Medical Management of Uterine Fibroids. 1999; 99-110.
  249. Kazmierczak B, Dal Cin P, Rogalla P, Van den Berghe H, Bullerdiek J. HMGI17 maps to chromosomal band 1p35 and is deleted in uterine leiomyomas with ring chromosome 1. 6th European Conference on Cytogenetics and Molecular Genetics of Human Solid Tumors. Cancer Genet Cytogenet. 1999; 122:83.
  250. Dal Cin P, Van den Berghe H, Buonamici L, Losi L, Roncaroli F, Calbucci F. Cytogenetic investigation in subependymoma. Cancer Genet Cytogenet. 1999 Jan 1; 108(1):84.
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  251. Kazmierczak B, Dal Cin P, Meyer-Bolte K, Van den Berghe H, Bullerdiek J. HMG1 is not the target of 13q12 rearrangements in lipomas. 6th European Conference on Cytogenetics and Molecular Genetics of Human Solid Tumors. Cancer Genet Cytogenet. 1999; (122):83-84.
  252. Dal Cin P, Van den Berghe H. Petrovich Z. Genetics of renal cell carcinoma. Carcinoma of the kidney, testis and uncommon tumors of the genitourinary tract. 1999.
  253. Dal Cin P., Van den Berghe H. . Cytogenetics of mesenchymal tumors of the uterus. Pathogenesis and Medical Management of Uterine Fibroids. 1999; 55-59.
  254. Dal Cin P, Van den Berghe H, Van Poppel H, Roskams T. Involvement of 12q12-13 is a nonrandom chromosome change in renal oncocytoma. Genes Chromosomes Cancer. 1999 Jan; 24(1):94.
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  255. Dal Cin P, Fusco A, Belge G, Chiappetta G, Fedele M, Pauwels P, Bullerdiek J, Van den Berghe H. . Involvement of HMGI(Y) gene in a microfollicular adenoma of thyroid. 6th European Conference on Cytogenetics and Molecular Genetics of Human Solid Tumors. Cancer Genet Cytogent. 1999; 122:76.
  256. Pedeutour F, Quade BJ, Weremowicz S, Dal Cin P, Ali S, Morton CC. Localization and expression of the human estrogen receptor beta gene in uterine leiomyomata. Genes Chromosomes Cancer. 1998 Dec; 23(4):361-6.
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  257. Van den Berghe H, Dal Cin P. Some genetic aspects of ovarian tumors. Eur J Obstet Gynecol Reprod Biol. 1998 Dec; 81(2):283-7.
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  258. Kazmierczak B, Dal Cin P, Wanschura S, Borrmann L, Fusco A, Van den Berghe H, Bullerdiek J. HMGIY is the target of 6p21.3 rearrangements in various benign mesenchymal tumors. Genes Chromosomes Cancer. 1998 Dec; 23(4):279-85.
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  259. Dei Tos AP, Dal Cin P, Sciot R, Furlanetto A, Da Mosto MC, Giannini C, Rinaldo A, Ferlito A. Synovial sarcoma of the larynx and hypopharynx. Ann Otol Rhinol Laryngol. 1998 Dec; 107(12):1080-5.
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  260. Losi L, Polito P, Hagemeijer A, Buonamici L, Van den Berghe H, Dal Cin P. Intracranial germ cell tumour (embryonal carcinoma with teratoma) with complex karyotype including isochromosome 12p. Virchows Arch. 1998 Dec; 433(6):571-4.
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  261. Dal Cin P, Gutierrez NC, Hernandez JM, Van den Berghe H. Molecular cytogenetics in angiomyolipomas. Cancer Genet Cytogenet. 1998 Oct 15; 106(2):182.
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  262. O'Brien KP, Seroussi E, Dal Cin P, Sciot R, Mandahl N, Fletcher JA, Turc-Carel C, Dumanski JP. Various regions within the alpha-helical domain of the COL1A1 gene are fused to the second exon of the PDGFB gene in dermatofibrosarcomas and giant-cell fibroblastomas. Genes Chromosomes Cancer. 1998 Oct; 23(2):187-93.
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  263. Polito P, Dal Cin P, Pauwels P, Christiaens M, Van den Berghe I, Moerman P, Vrints L, Van den Berghe H. An important subgroup of phyllodes tumors of the breast is characterized by rearrangements of chromosomes 1q and 10q. Oncol Rep. 1998 Sep-Oct; 5(5):1099-102.
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  264. Sciot R, Dal Cin P, Bellemans J, Samson I, Van den Berghe H, Van Damme B. Synovial chondromatosis: clonal chromosome changes provide further evidence for a neoplastic disorder. Virchows Arch. 1998 Aug; 433(2):189-91.
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  265. Balzarini P, Dal Cin P, Roskams T, Polito P, Van Poppel H, Van Damme B, Baert L, Van den Berghe H. Histology may depend on the presence of partial monosomy or partial trisomy 3 in renal cell carcinoma. Cancer Genet Cytogenet. 1998 Aug; 105(1):6-10.
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  266. Dal Cin P, Vanni R, Polito P, Van den Berghe H. [Diagnostic impact of cytogenetics for solid tumors]. Pathologica. 1998 Aug; 90(4):337-42.
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  267. Dal Cin P, Sciot R, Samson I, De Wever I, Van den Berghe H. Osteoid osteoma and osteoblastoma with clonal chromosome changes. Br J Cancer. 1998 Aug; 78(3):344-8.
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  268. Dal Cin P, Timmerman D, Van den Berghe I, Wanschura S, Kazmierczak B, Vergote I, Deprest J, Neven P, Moerman P, Bullerdiek J, Van den Berghe H. Genomic changes in endometrial polyps associated with tamoxifen show no evidence for its action as an external carcinogen. Cancer Res. 1998 Jun 1; 58(11):2278-81.
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  269. Dal Cin P, Wanschura S, Kazmierczak B, Tallini G, Dei Tos A, Bullerdiek J, Van den Berghe I, Moerman P, Van den Berghe H. Amplification and expression of the HMGIC gene in a benign endometrial polyp. Genes Chromosomes Cancer. 1998 Jun; 22(2):95-9.
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  270. Dal Cin P, Sciot R, Fletcher CD, Samson I, De Vos R, Mandahl N, Willén H, Larsson O, Van den Berghe H. Inflammatory leiomyosarcoma may be characterized by specific near-haploid chromosome changes. J Pathol. 1998 May; 185(1):112-5.
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  271. Dal Cin P, Sciot R, De Smet L, Van den Berghe H. Translocation 2;11 in a fibroma of tendon sheath. Histopathology. 1998 May; 32(5):433-5.
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  272. Mertens F, Fletcher CD, Dal Cin P, De Wever I, Mandahl N, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van den Berghe H, Vanni R, Willén H. Cytogenetic analysis of 46 pleomorphic soft tissue sarcomas and correlation with morphologic and clinical features: a report of the CHAMP Study Group. Chromosomes and MorPhology. Genes Chromosomes Cancer. 1998 May; 22(1):16-25.
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  273. Dal Cin P, Lipcsei G, Hermand G, Boniver J, Van den Berghe H. Congenital mesoblastic nephroma and trisomy 11. Cancer Genet Cytogenet. 1998 May; 103(1):68-70.
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  274. Dal Cin P, Pauwels P, Van den Berghe H. Fibrosarcoma versus cellular fibroma of the ovary. Am J Surg Pathol. 1998 Apr; 22(4):508-10.
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  275. Dal Cin P, Polito P, Van den Berghe H. [Genetics of renal tumors]. Pathologica. 1998 Apr; 90(2):101-7.
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  276. Willén H, Akerman M, Dal Cin P, De Wever I, Fletcher CD, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van den Berghe H, Vanni R. Comparison of chromosomal patterns with clinical features in 165 lipomas: a report of the CHAMP study group. Cancer Genet Cytogenet. 1998 Apr 1; 102(1):46-9.
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  277. Buonamici L, Roncaroli F, Frank G, Dal Cin P, Van den Berghe H, Calbucci F, Eusebi V. [Cytogenetic analysis of hypophyseal adenoma. Study of 9 cases and review of the literature]. Pathologica. 1998 Apr; 90(2):116-9.
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  278. Dal Cin P, Pauwels P, Moerman P, Qi H, Van Den Berghe H. Hyperdiploidy in benign breast lesions. Cancer Genet Cytogenet. 1998 Mar; 101(2):162-3.
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  279. Kazmierczak B, Dal Cin P, Wanschura S, Bartnitzke S, Van den Berghe H, Bullerdiek J. Cloning and molecular characterization of part of a new gene fused to HMGIC in mesenchymal tumors. Am J Pathol. 1998 Feb; 152(2):431-5.
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  280. Brosens I, Deprest J, Dal Cin P, Van den Berghe H. Clinical significance of cytogenetic abnormalities in uterine myomas. Fertil Steril. 1998 Feb; 69(2):232-5.
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  281. Dal Cin P, Stas M, Sciot R, De Wever I, Van Damme B, Van den Berghe H. Translocation (X;1) reveals metastasis 31 years after renal cell carcinoma. Cancer Genet Cytogenet. 1998 Feb; 101(1):58-61.
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  282. Dei Tos A.P., Doglioni C., Piccinin S., Furlanetto A., Sciot R., Dal Cin P., Boiocchi M., Fletcher C.D.P., Tallini G. Coordinated expression of MDM2, CDK4 and HMGI-C in atypical lipomatous tumors. United States and Canadian Academy of Pathology. 1998; Boston, MA.
  283. Dal Cin P, Dei Tos AP, Qi H, Giannini C, Furlanetto A, Longatti PL, Marynen P, Van den Berghe H. Immature teratoma of the pineal gland with isochromosome 12p. Acta Neuropathol. 1998 Jan; 95(1):107-10.
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  284. Dal Cin P. Cytogenetics of soft tissue tumours. Verh Dtsch Ges Pathol. 1998; 82:47-58.
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  285. Dal Cin P. . Cytogenetics of soft tissue tumours. Proceedings of the German Society of Pathology. 1998; 82:47-58.
  286. Dal Cin P, Polito P, Van den Berghe H. Genetica dei tumori renali. Pathologica. 1998; 90:101-07..
  287. Dal Cin P, Qi H, Pauwels P, Backx C, Van den Berghe H. Monosomy 22 in a fibrothecoma. Cancer Genet Cytogenet. 1997 Dec; 99(2):129-31.
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  288. Dal Cin P, Sciot R, Van Poppel H, Baert L, Van Damme B, Van den Berghe H. Chromosome analysis in angiomyolipoma. Cancer Genet Cytogenet. 1997 Dec; 99(2):132-4.
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  289. Dal Cin P, Sciot R, Fletcher CDM, De Vos R, Mandahl N, Willén H, Larson O, Van den Berghe,H. . Near-haploidy may characterize inflammatory leiomyosarcoma as a distinct entity. CTOS 3rd Annual Scientific Meeting. 1997; Milano, Italy.
  290. Sciot R, Dal Cin P, Fletcher CD, Hernandez JM, Garcia JL, Samson I, Ramos L, Brys P, Van Damme B, Van den Berghe H. Inflammatory myofibroblastic tumor of bone: report of two cases with evidence of clonal chromosomal changes. Am J Surg Pathol. 1997 Oct; 21(10):1166-72.
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  291. Dal Cin P, Polito P, Van Eyken P, Sciot R, Hernandez JM, Garcia JL, Van den Berghe H. Anomalies of chromosomes 17 and 22 in giant cell fibroblastoma. Cancer Genet Cytogenet. 1997 Sep; 97(2):165-6.
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  292. Dal Cin P, Sciot R, Polito P, Stas M, de Wever I, Cornelis A, Van den Berghe H. Lesions of 13q may occur independently of deletion of 16q in spindle cell/pleomorphic lipomas. Histopathology. 1997 Sep; 31(3):222-5.
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  293. Dal Cin P, Wanschura S, Christiaens MR, Van den Berghe I, Moerman P, Polito P, Kazmierczak B, Bullerdiek J, Van den Berghe H. Hamartoma of the breast with involvement of 6p21 and rearrangement of HMGIY. Genes Chromosomes Cancer. 1997 Sep; 20(1):90-2.
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  294. Dei Tos AP, Dal Cin P. The role of cytogenetics in the classification of soft tissue tumours. Virchows Arch. 1997 Aug; 431(2):83-94.
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  295. Dal Cin P, Sciot R, Panagopoulos I, Aman P, Samson I, Mandahl N, Mitelman F, Van den Berghe H, Fletcher CD. Additional evidence of a variant translocation t(12;22) with EWS/CHOP fusion in myxoid liposarcoma: clinicopathological features. J Pathol. 1997 Aug; 182(4):437-41.
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  296. Dal Cin P, Van den Berghe H, Sciot R, de Wever I. Deletion of the long arm of chromosome 7 in lipoma. Cancer Genet Cytogenet. 1997 Jul 1; 96(1):85-6.
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  297. Tallini G, Dal Cin P, Rhoden KJ, Chiapetta G, Manfioletti G, Giancotti V, Fusco A, Van den Berghe H, Sciot R. Expression of HMGI-C and HMGI(Y) in ordinary lipoma and atypical lipomatous tumors: immunohistochemical reactivity correlates with karyotypic alterations. Am J Pathol. 1997 Jul; 151(1):37-43.
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  298. Dal Cin P, Van den Berghe H. Ten years of the cytogenetics of soft tissue tumors. Cancer Genet Cytogenet. 1997 May; 95(1):59-66.
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  299. Dal Cin P, Sciot R, Kazmierczak B, Wanschura S, Samson I, Van Poppel H, Van den Berghe H, Bullerdiek J. Inflammatory pseudotumors with HMGIC rearrangement. Fourth International Workshop (SCW12.4) on chromosome 12. 1997; Nice, France.
  300. Van den Hove LE, Van Gool SW, Van Poppel H, Baert L, Coorevits L, Van Damme B, Dal Cin P, Van den Berghe H, Ceuppens JL. Identification of an enriched CD4+ CD8alpha++ CD8beta+ T-cell subset among tumor-infiltrating lymphocytes in human renal cell carcinoma. Int J Cancer. 1997 Apr 10; 71(2):178-82.
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  301. Sciot R, Akerman M, Dal Cin P, De Wever I, Fletcher CD, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Tallini G, Van den Berghe H, Vanni R, Willen H. Cytogenetic analysis of subcutaneous angiolipoma: further evidence supporting its difference from ordinary pure lipomas: a report of the CHAMP Study Group. Am J Surg Pathol. 1997 Apr; 21(4):441-4.
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  302. Wanschura S, Dal Cin P, Kazmierczak B, Bartnitzke S, Van den Berghe H, Bullerdiek J. Hidden paracentric inversions of chromosome arm 12q affecting the HMGIC gene. Genes Chromosomes Cancer. 1997 Apr; 18(4):322-3.
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  303. Vanni R, Marras S, Schoenmakers EF, Dal Cin P, Kazmierczak B, Senger G, Bullerdiek J, Van de Ven WJ, Van den Berghe H. Molecular cytogenetic characterization of del(7q) in two uterine leiomyoma-derived cell lines. Genes Chromosomes Cancer. 1997 Mar; 18(3):155-61.
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  304. Tallini G, Dal Cin P, Giancotti V, Fusco A, Van den Berghe H, Sciot R. Expression of HMGI-C and HMGI(Y) in lipoma and atypical lipomatous tumors; immunohistochemical reactivity correlates with karyotypic alterations. United States and Canadian Academy of Pathology 86th Annual Meeting. 1997; Orlando,FL.
  305. Dal Cin P, Qi H, Sciot R, Van den Berghe H. Involvement of chromosomes 6 and 11 in a soft tissue chondroma. Cancer Genet Cytogenet. 1997 Feb; 93(2):177-8.
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  306. Hernández JM, Schoenmakers EF, Dal Cin P, Michaux L, Van de Ven WJ, Van den Berghe H. Molecular delineation of the commonly deleted segment in mature B-cell lymphoid neoplasias with deletion of 7q. Genes Chromosomes Cancer. 1997 Feb; 18(2):147-50.
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  307. Dal Cin P, Van den Berghe H. Chromosomal abnormalities in adipose tissue tumors. Lipomatous Tumors: Diagnosis and Primary Treatment. Surgical Oncology Series. 1997; 4:31-41.
  308. Dal Cin P, Wanschura, Moerman,Ph. Sciot R, Christiaens MR, Kazmierczak B, Bullerdiek J, Van den Berghe H. Different breast tumors with involvement of different HMG genes in the same patient. 7th International Workshop on Chromosomes in Solid Tumors. Cancer Genet Cytogenet. 1997; 98:157.
  309. Dal Cin P, Wanschura S, Kazmierczak B, Bullerdiek J, Van den Berghe I, Moerman Ph, Van den Berghe H. Amplification of HMGIC in an endometrial polyp. 7th International Workshop on Chromosomes in Solid Tumors. Cancer Genet Cytogenet. 1997; (98):158.
  310. Wanschura S, Dal Cin P, Kazmierczak B. Bartnitzke S, Van Den Berghe H., Bullerdiek, J. Hidden paracentric inversions of chromosome 12q affecting the HMGIC gene. 7th International Workshop on Chromosomes in Solid Tumors. Cancer Genet Cytogenet. 1997; (98):168.
  311. Dal Cin P, Sciot R, Panagopoulos I, Åman P, Samson I, Mandahl N, Mitelman F, Van den Berghe H, Fletcher CDM. Additional evidence of a variant translocation t(12;22) with EWS/CHOP fusion in myxoid liposarcoma: clinicopathological features. 7th International Workshop on Chromosomes in Solid Tumors. Cancer Genet Cytogenet. 1997; 98:157.
  312. Kazmierczak B, Wanschura S, Dal Cin P, Van den Berghe H, Bullerdiek J. Involvement of the HMGIY gene in mesenchymal tumors with 6p21 aberrations. 7th International Workshop on Chromosomes in Solid Tumors. Cancer Genet Cytogenet. 1997; (98):151.
  313. Qi H, Dal Cin P, Hernández JM, Garcia JL, Sciot R, Fletcher C, Van Eyken P, De Wever I, Van den Berghe H. Trisomies 8 and 20 in desmoid tumors. Cancer Genet Cytogenet. 1996 Dec; 92(2):147-9.
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  314. Cuneo A, Ferrant A, Michaux JL, Bosly A, Chatelain B, Stul M, Dal Cin P, Dierlamm J, Cassiman JJ, Hossfeld DK, Castoldi G, Van den Berghe H. Cytogenetic and clinicobiological features of acute leukemia with stem cell phenotype: study of nine cases. Cancer Genet Cytogenet. 1996 Nov; 92(1):31-6.
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  315. Dal Cin P, Marynen P, Moerman P, Vergot I, Van den Berghe H. Ovarian germ cell tumor with chromosome 12 anomaly but without i(12p). Cancer Genet Cytogenet. 1996 Oct 1; 91(1):61-4.
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  316. Dal Cin P, Van Poppel H, Sciot R, De Vos R, Van Damme B, Baert L, Van den Berghe H. The t(1;12)(p36;q13) in a renal oncocytoma. Genes Chromosomes Cancer. 1996 Oct; 17(2):136-9.
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  317. Rosai J, Akerman M, Dal Cin P, DeWever I, Fletcher CD, Mandahl N, Mertens F, Mitelman F, Rydholm A, Sciot R, Tallini G, Van den Berghe H, Van de Ven W, Vanni R, Willen H. Combined morphologic and karyotypic study of 59 atypical lipomatous tumors. Evaluation of their relationship and differential diagnosis with other adipose tissue tumors (a report of the CHAMP Study Group). Am J Surg Pathol. 1996 Oct; 20(10):1182-9.
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  318. Mandahl N, Akerman M, Aman P, Dal Cin P, De Wever I, Fletcher CD, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van den Berghe H, Van de Ven W, Vanni R, Willén H. Duplication of chromosome segment 12q15-24 is associated with atypical lipomatous tumors: a report of the CHAMP collaborative study group. CHromosomes And MorPhology. Int J Cancer. 1996 Sep 4; 67(5):632-5.
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  319. Tallini G, Akerman M, Dal Cin P, De Wever I, Fletcher CD, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Van den Berghe H, Van den Ven W, Vanni R, Willen H. Combined morphologic and karyotypic study of 28 myxoid liposarcomas. Implications for a revised morphologic typing, (a report from the CHAMP Group). Am J Surg Pathol. 1996 Sep; 20(9):1047-55.
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  320. Brosens I, Johannisson E, Dal Cin P, Deprest J, Van den Berghe H. Analysis of the karyotype and desoxyribonucleic acid content of uterine myomas in premenopausal, menopausal, and gonadotropin-releasing hormone agonist-treated females. Fertil Steril. 1996 Sep; 66(3):376-9.
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  321. Cuneo A, Ferrant A, Michaux JL, Demuynck H, Boogaerts M, Louwagie A, Doyen C, Stul M, Cassiman JJ, Dal Cin P, Castoldi G, Van den Berghe H. Philadelphia chromosome-positive acute myeloid leukemia: cytoimmunologic and cytogenetic features. Haematologica. 1996 Sep-Oct; 81(5):423-7.
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  322. Dal Cin P, Pauwels P, Van de Moosdijk CNF, Vrints L, Sciot R, Van den Berghe. Cytogenetics revealing the diagnosis in a metastatic endometrial stromal sarcoma. 9th International Congress of Human Genetics. 1996; Rio de Janeiro, Brazil.
  323. Dal Cin P, De Wolf-Peeters C, Deneffe G, Fryns JP, Van den Berghe H. Thymoma with a t(15;22)(p11;q11). Cancer Genet Cytogenet. 1996 Jul 15; 89(2):181-3.
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  324. Dal Cin P, Sciot R, De Wever I, Van Damme B, Van den Berghe H. Diagnosis of primary renal cell carcinoma in a left supraclavicular lymph node by chromosome analysis. J Urol. 1996 Jul; 156(1):171-2.
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  325. Dal Cin P, van Poppel H, van Damme B, Baert L, Van den Berghe H. Cytogenetic investigation of synchronous bilateral renal tumors. Cancer Genet Cytogenet. 1996 Jul 1; 89(1):57-60.
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  326. Pauwels P, Dal Cin P, Van de Moosdijk CN, Vrints L, Sciot R, Van den Berghe H. Cytogenetics revealing the diagnosis in a metastatic endometrial stromal sarcoma. Histopathology. 1996 Jul; 29(1):84-7.
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  327. Cuneo A, Castoldi G, Michaux JL, Ferrant A, Chatelain B, Louwagie A, St Jan AZ, Boogaerts M, Dal Cin P, Van den Berghe H. Differences in the chromosomal profile of AML-M0 versus AML-M1: response. Blood. 1996 Jun 15; 87(12):5381-2.
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  328. Dal Cin P, Moerman P, Christiaens MR, Van den Berghe H. Observation of a deletion of the long arm of chromosome 6 in benign fibrocystic disease of the breast constitutes a challenging problem. Genes Chromosomes Cancer. 1996 May; 16(1):68-71.
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  329. Dal Cin P, Sciot R, Pauwels P, De Wever I, Van den Berghe H. Cytogenetics revealing the diagnosis in metastases of unknown origin. 5th European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. 1996; Baveno - Stresa, Italy.
  330. Kazmierczak B, Dal Cin P, Vanni R, Bartnitzke S, Van den Berghe H, Bullerdiek J. . Failure to establish cell lines from uterine leiopmyomas showing the del(7) as the sole abnormality. 5th European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. 1996; Baveno - Stresa, Italy.
  331. Dal Cin P, Marynen P, Moerman PH, Vergote I, Van den Berghe H. Ovarium germ cell tumor with chromosome 12 anomaly but without i(12p). 5th European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. 1996; Baveno - Stresa, Italy.
  332. Qi H, Dal Cin P, Van de Voorde W, Van Poppel H, Baert L, Van den Berghe H. Cytogenetic and fish study in 120 cases of prostate adenocarcinoma. 5th European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. 1996; Baveno - Stresa, Italy.
  333. Vanni R, Marras S, Dal Cin P, Schoenmakers E, Kazmierckzak B, Bullerdiek J, Van de Ven JWJ, Van den Berghe H. . In situ fluorescence hybridization analysis of deletion of the long arm of chromosome 7 in a uterine leiomyoma derived cell line. 5th European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. 1996; Baveno - Stresa, Italy.
  334. Dal Cin P, Van Poppel H, Van Damme B, Baert L, Van den Berghe H. Cytogenetic investigation Of synchronous bilateral renal tumors. 5th European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. 1996; Baveno - Stresa, Italy.
  335. Qi H, Dal Cin P, García JL, Hernández JM, Van den Berghe H. Trisomy 8 and trisomy 20 in desmoid tumours. 5th European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. 1996; Baveno - Stresa, Italy.
  336. Dal Cin P, Pauwels P, Sciot R, Van den Berghe H. Multiple chromosome rearrangements in a fibrosarcoma. Cancer Genet Cytogenet. 1996 Apr; 87(2):176-8.
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  337. Dal Cin P, Scoit R, De Smet L, Van Damme B, Van Den Berghe H. A new cytogenetic subgroup in tenosynovial giant cell tumors (nodular tenosynovitis) is characterized by involvement of 16q24. Cancer Genet Cytogenet. 1996 Mar; 87(1):85-7.
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  338. Qi H, Dal Cin P, Van de Voorde W, Elgamal AA, Van Poppel H, Baert L, Van Den Berghe H. del(1)(q12) in adenocarcinomas of the prostate. Cancer Genet Cytogenet. 1996 Mar; 87(1):79-81.
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  339. Brosens IA, Johannisson E, Dal Cin P, Deprest J, Van den Berghe H. Proliferation rate and oestrogen dependency of uterine leiomyomas are dependent on the chromosomal pattern. 4th International Symposium on GnRH Analogues in Cancer and Human Reproduction. 1996; Geneva, Switzerland.
  340. Fletcher CD, Akerman M, Dal Cin P, de Wever I, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, van den Berghe H, van de Ven W, Vanni R, Willen H. Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group. Am J Pathol. 1996 Feb; 148(2):623-30.
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  341. Dal Cin P, Sciot R, Fletcher CD, Hilliker C, De Wever I, Van Damme B, Van den Berghe H. Trisomy 21 in solitary fibrous tumor. Cancer Genet Cytogenet. 1996 Jan; 86(1):58-60.
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  342. Cuneo A, Ferrant A, Michaux JL, Chatelain B, Stul, M, Dal Cin P, Begoni R., Matteo Rigolin G, Castoldi ., Van den Berghe, H. Cytogenetic and clinicobiologic features of acute undifferentiated leukemia with stem cell phenotype. Study of nine cases. Second Meeting of the European Haematology Association. Brit J Haematol. Suppl 2. 1996; (93):327.
  343. Dal Cin P, Van den Berghe H. Chromosome abnormalities in adenocarcinoma of the prostate. Carcinoma of the Prostate. Innovations in Management. 1996; 51-54.
  344. García JL, Hernández JM, González M, San Miguel JF, Dal Cin P, Van Den Berghe H. Translocation (15;17)(q22;q21) in a patient with Klinefelter syndrome. Cancer Genet Cytogenet. 1996 Jan; 86(1):86.
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  345. Dal Cin P, Sciot R, de Wever I, Brock P, Casteels-Van Daele M, Van Damme B, Van Den Berghe H. Cytogenetic and immunohistochemical evidence that giant cell fibroblastoma is related to dermatofibrosarcoma protuberans. Genes Chromosomes Cancer. 1996 Jan; 15(1):73-5.
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  346. Hernández JM, Michaux L, Schoenmakers EFPM, Dal Cin P, Criel A, Van Orshoven A, De Wolf-Peeters C, Van de Ven WJM, Mecucci C, Van den Berghe H. Clinical, biological and molecular characterization of del(7)(q) in B-cell chronic lymphoid malignancies.Second Meeting of the European Haematology Association. Brit. J. Haematol. 93. 1996; (Suppl. 2):283.
  347. Wanschura S, Belge G, Stenman G, Kools P, Dal Cin P, Schoenmakers E, Huysmans C, Van den Berghe H, Bartnitzke S, Van de Ven WJ, Bullerdiek J. Mapping of the translocation breakpoints of primary pleomorphic adenomas and lipomas within a common region of chromosome 12. Cancer Genet Cytogenet. 1996 Jan; 86(1):39-45.
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  348. Dal Cin P, Van Poppel H, Sciot R, De Vos R, Van Damme B, Baert L, Van den Berghe H. t(1;12)(p36;q13) in a renal oncocytoma.Chromosome 12 Genes in Cancer. 1995; Leuven, Belgium.
  349. Kools PFJ, De Wever I, Sciot R, Dal Cin P, Van den Berghe H, Van de Ven WJM. Amplifiaction of the high mobility group protein gene HMGI-C in atypical lipomatous tumors. Chromosome 12 Genes in Cancer. 1995; Leuven, Belgium.
  350. Sciot R, Dal Cin P, Fletcher CD, De Wever I, De Vos R, Van Damme B, Van den Berghe H. Monosomy 22 in a malignant peripheral nerve sheath tumour of the kidney in childhood: a genetic link with other malignant paediatric renal neoplasms? Histopathology. 1995 Oct; 27(4):373-6.
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  351. Dal Cin P, Sciot R, Fletcher CDM, Hilliker C, De Wever I, Van Damme B, Van den Berghe H. . Trisomy 21 in solitary fibrous tumor. 12th International Chromosome Conference. 1995; Madrid, Spain.
  352. Dal Cin P, Moreman P, De Wever I, Van den Berghe H. Is i(1)(q10) a chromosome marker in phyllodes tumor of the breast? Cancer Genet Cytogenet. 1995 Sep; 83(2):174-5.
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  353. Sciot R, Dal Cin P, Fletcher C, Samson I, Smith M, De Vos R, Van Damme B, Van den Berghe H. t(9;22)(q22-31;q11-12) is a consistent marker of extraskeletal myxoid chondrosarcoma: evaluation of three cases. Mod Pathol. 1995 Sep; 8(7):765-8.
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  354. De Smet L, Dal Cin P, Van Damme B. Cytogenetic characterization of tenosynovial giant cell tumors. M. Vastamäki, S. Vilkki, H. Goransson, H. Jaroma, T. Raatikainen & T. Viliakka (eds.), 6th Congress of the International Federation of Societies for Surgery of the Hand (IFSSH); Monduzzi Editore, International Proceedings Division. 1995; 937.
  355. Sciot R, Samson I, Dal Cin P, Lateur L, van Damme B, van den Berghe H, Desmet V. Giant cell rich parosteal osteosarcoma. Histopathology. 1995 Jul; 27(1):51-5.
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  356. Dal Cin P, Moerman P, Deprest J, Brosens I, Van den Berghe H. A new cytogenetic subgroup in uterine leiomyoma is characterized by a deletion of the long arm of chromosome 3. Genes Chromosomes Cancer. 1995 Jul; 13(3):219-20.
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  357. Cuneo A, Ferrant A, Michaux JL, Boogaerts M, Demuynck H, Van Orshoven A, Criel A, Stul M, Dal Cin P, Hernandez J, et al. Cytogenetic profile of minimally differentiated (FAB M0) acute myeloid leukemia: correlation with clinicobiologic findings. Blood. 1995 Jun 15; 85(12):3688-94.
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  358. Uyttebroeck A, Brock P, De Groote B, Renard M, Dal Cin P, Van den Berghe H, Casteels-Van Daele M. 5q- syndrome in a child. Cancer Genet Cytogenet. 1995 Apr; 80(2):121-3.
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  359. Dal Cin P, Vanni R, Marras S, Moerman P, Kools P, Andria M, Valdes E, Deprest J, Van de Ven W, Van den Berghe H. Four cytogenetic subgroups can be identified in endometrial polyps. Cancer Res. 1995 Apr 1; 55(7):1565-8.
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  360. Dal Cin P, Sciot R, Van Damme B, De Wever I, Van den Berghe H. Trisomy 20 characterizes a second group of desmoid tumors. Cancer Genet Cytogenet. 1995 Feb; 79(2):189.
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  361. Wanschura, S., Belge G, Stenman G, Schoenmakers, E, Dal Cin P, Bartnitzka, S., Van den Berghe, H., Van de Ven, W., Bullerdiek, J. Physical mapping of 12q13-q15 translocation breakpoints of primary pleomorphic adenomas of the salivary glands, uterine leiomyomas, lipomas and derived cell lines. 6th International Workshop on Chromosomes in Solid Tumors February 19-21. Cancer Genet Cytogenet. 1995; (84):141.
  362. Renwick PJ, Reeves BR, Dal Cin P, Fletcher CD, Kempski H, Sciot R, Kazmierczak B, Jani K, Sonobe H, Knight JC. Two categories of synovial sarcoma defined by divergent chromosome translocation breakpoints in Xp11.2, with implications for the histologic sub-classification of synovial sarcoma. Cytogenet Cell Genet. 1995; 70(1-2):58-63.
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  363. Cuneo A, Ferrant A, Michaux JL, Boogaerts M, Demuynck H, Bosly A, Doyen C, Carli G, Piva N, Castoldi G, Stul M, Dal Cin P, Cassiman JJ, Van den Berghe H. Clinical review on features and cytogenetic patterns in adult acute myeloid leukemia with lymphoid markers. Leukemia & Lymphoma Review Series. 1995; 13-19.
  364. Dal Cin P, Vanni R, Marras S, Moerman PH, Kools P, Andria M, Valdes E, Deprest J, Van den Berghe H, Van de Ven W. Four cytogenetic subgroups can be identified in endometrial polyps. 6th International Workshop on Chromosomes in Solid Tumors. Cancer Genet Cytogenet. 1995; (84):153.
  365. 87. Tallini G, Dal Cin P, De Wever I, Fletcher CDM, Mandahl N, Mertens F Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van den Berghe H, Vanni R, Willén H; Yale U., New Haven, CT; Memorial Sloan-Ketterinc Cancer Center, NY, NY; Guy's and St. Thomas' Hosp., London, U.; U. of Lund, Sweden; U. of Leuven, Belgium; and U. of Cagliari, Italy. Myxoid liposarcoma represents a distinct type of liposarcoma characterized by the specific cytogenetic translocation t(12;16)(q13;p11). 1995 Annual Meeting United States and Canadian Academy of Pathology. 1995; Toronto, Canada.
  366. Sciot R, De Vos R, Dal Cin P. Morfologische, immunohistochemische en cytogenetische studie van gastro-intestinale stromale tumoren. Tijdschr. Gastroenterol. 1995; 7-10.
  367. Sciot R, Dal Cin P, Samson I, Smith M., Fletcher C. t(9;22)(q22-31;q11-12) is a consistent marker of extraskeletal myxoid chondrosarcoma. evalution of 3 cases. United States and Canadian Academy of Pathology. 1995; Toronto, Canada.
  368. Sciot R, Dal Cin P, Fletcher CDM, De Wever I, Van den Berghe H. Monosomy of chromosome 22 in a malignant peripheral nerve sheath tumor of the kidney. 6th International Workshop on Chromosomes in Solid Tumors. 1995; Tucson, AZ.
  369. Knight JC, Renwick PJ, Dal Cin P, Van den Berghe H, Fletcher CD. Translocation t(12;16)(q13;p11) in myxoid liposarcoma and round cell liposarcoma: molecular and cytogenetic analysis. Cancer Res. 1995 Jan 1; 55(1):24-7.
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  370. Dal Cin P, Sciot R, De Wever I, Van Damme B, Van den Berghe H. Trisomy 21 in a solitary fibrous tumor. 86th Annual Meeting of the American Association for Cancer Research. 1995; Toronto, Canada.
  371. Van den Berghe H, Dal Cin P. Chromosomes and Cancer. Oxford Textbook of Oncology. 1995.
  372. Tallini G, Dal Cin P, De Wever I, Fletcher CDM, Mandahl N, Mertens F Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van den Berghe H, Vanni R, Willén H; Yale U., New Haven, CT; Memorial Sloan-Ketterinc Cancer Center, NY, NY; Guy's and St. Thomas' Hosp., London, U.; U. of Lund, Sweden; U. of Leuven, Belgium; and U. of Cagliari, Italy. . Atypical lipomatous tumors. evalutation of their relatinship and differential diagnosis with other adipose tissue tumors based on a combined morphologic-karyotypic study of cases. 1995 Annual Meeting United States and Canadian Academy of Pathology. 1995; Toronto, Canada.
  373. Dei Tos AP, Calonje E, Sciot R, Pauwels P, Knight JC, Dal Cin P, Fletcher CD. Immunohistochemical demonstration of glycoprotein p30/32MIC2 (CD99) in synovial sarcoma. A potential cause of diagnostic confusion. App Immunhistochem. 1995; 3:168-73.
  374. Dal Cin P, Sciot R, De Wever I, Van Damme B, Van den Berghe H. New discriminative chromosomal marker in adipose tissue tumors. The chromosome 8q11-q13 region in lipoblastoma. Cancer Genet Cytogenet. 1994 Dec; 78(2):232-5.
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  375. Dal Cin P, Sciot R, Speleman F, Samson I, Laureys G, de Potter C, Meire F, van Damme B, van den Berghe H. Chromosome aberrations in fibrous dysplasia. Cancer Genet Cytogenet. 1994 Oct 15; 77(2):114-7.
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  376. Dal Cin P, Sciot R, Samson I, De Smet L, De Wever I, Van Damme B, Van den Berghe H. Cytogenetic characterization of tenosynovial giant cell tumors (nodular tenosynovitis). Cancer Res. 1994 Aug 1; 54(15):3986-7.
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  377. Cuneo A, Demuynck H, Ferrant A, Louwagie A, Doyen C, Stul M, Cassiman JJ, Dal Cin P, Negrini M, Carli MG, et al. Minor myeloid component in Ph chromosome-positive acute lymphoblastic leukaemia: correlation with cytogenetic pattern and implication for poor response to therapy. Br J Haematol. 1994 Jul; 87(3):515-22.
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  378. Sciot R, Dal Cin P, Brock P, Moerman P, Van Damme B, De Wever I, Casteels-Van Daele M, Van den Berghe H, Desmet V. Pleuropulmonary blastoma (pulmonary blastoma of childhood): genetic link with other embryonal malignancies? Histopathology. 1994 Jun; 24(6):559-63.
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  379. Dal Cin P, Sciot R, Aly MS, Delabie J, Stas M, De Wever I, Van Damme B, Van den Berghe H. Some desmoid tumors are characterized by trisomy 8. Genes Chromosomes Cancer. 1994 Jun; 10(2):131-5.
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  380. Aly MS, Dal Cin P, Van de Voorde W, van Poppel H, Ameye F, Baert L, Van den Berghe H. Chromosome abnormalities in benign prostatic hyperplasia. Genes Chromosomes Cancer. 1994 Apr; 9(4):227-33.
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  381. Schoenmakers EF, Kools PF, Mols R, Kazmierczak B, Bartnitzke S, Bullerdiek J, Dal Cin P, De Jong PJ, Van den Berghe H, Van de Ven WJ. Physical mapping of chromosome 12q breakpoints in lipoma, pleomorphic salivary gland adenoma, uterine leiomyoma, and myxoid liposarcoma. Genomics. 1994 Mar 15; 20(2):210-22.
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  382. Aly MS, Dal Cin P, Jiskoot P, Deneffe G, Marynen P, Van den Berghe H. Competitive in situ hybridization in a mediastinal germ cell tumor. Cancer Genet Cytogenet. 1994 Mar; 73(1):53-6.
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  383. De Wever I, Ectors N, Haustermans K, Dal Cin P, Stas M, Dubin M, Geboes K. Clinical and histological progression of a diploid pseudomyxoma peritonei of appendical origin. Belgian Week of Gatroenterology. 1994; Knokke, Belgium.
  384. Schoenmakers EFPM, Kools PFJ, Mols R, Kazmierczak B, Bartnitzke S, Bullerdiek J, Dal Cin P, Van den Berghe H, Van de Ven WJM. . Physical mapping of chromosome 12q translocation breakpoints in one malignant and three benign solid tumors. 4th European Workshop on Cytogenetics and Molecular Genetics of Human Solid tumors. Cancer Genet Cytogenet. 1994; (77):201.
  385. Kools PFJ, Dal Cin P, Schoenmakers FPM, Van den Berghe H, Van de Ven WJM. FISH studies on ring and long-marker chromosomes from atypical lipomas and well-differentiated liposarcomas reveal involvement of region 12q13-q15. 4th European Workshop on Cytogenetics and Molecular Genetics of Human Solid tumors. Cancer Genet Cytogenet. 1994; (77):161.
  386. Dal Cin P, Van den Berghe H. Innovations in the Management of Benign Prostatic Hyperplasia. Chromosome abnormalities in benign prostatic hyperplasia. Heidelberg:. Petrovich Z, Baert L, eds Springer Verlag. 1994; 49-56.
  387. Van Poppel H, Dal Cin P, Aly MS, Van Damme B, Van den Berghe H, Baert L. . Trisomy 7 and trisomy 10 in the healthy parenchyma of RCC bearing kidneys is not a premalignant lesion. XIth Congress of the European Association of Urology. 1994; Berlin, Germany.
  388. Vanni R, Dal Cin P, Kazmierczak B, Marras S, Bullerdiek J, Van de Ven W, Van den Berghe H. . Loss of the c-Met proto-oncogene from the deleted chromosome 7 of a uterine leiomyoma cell line. 4th European Workshop on Cytogenetics and Molecular Genetics of Human Solid tumors. Cancer Genet Cytogenet. 1994; (77):203.
  389. Aly MS, Dal Cin P, Van Damme B, Van Poppel H, Baert L, Van den Berghe H. Cytogenetic study of renal cell carcinoma. 4th European Workshop on Cytogenetics and Molecular Genetics of Human Solid tumors. Cancer Genet Cytogenet. 1994; (77):191.
  390. Vanni R, Dal Cin P. Involvement of chromosome 12 in uterine leiomyoma. . Chromosome 12 Aberrations in Human Solid Tumors. Cytogenetics and Molecular Genetics. 1994; 16-26.
  391. Van Poppel H, Dal Cin P, Aly MS, Van Damme B, Van den Berghe H, Baert L. Non-papillary renal cell carcinoma is characterized by monosmy 3p and papillary renal cell carcinoma by trisomy 17 and other chromosome changes. XIth Congress of the European Association of Urology. 1994; Berlin, Germany.
  392. Kazmierczak B, Bartnitzke S, Dal Cin P, Vanni R, Bullerdiek J. . Cell lines from tumours showing 12q13-15 aberrations. Chromosome 12 Aberrations in Human Solid Tumors. Cytogenetics and Molecular Genetics. 1994; 89-102.
  393. Herrmann ME, Belge G, Stern C, Dal Cin P, Bullerdiek J, Bartnitzke S. Breakpoints and recipient chromosomes in pleomorphic adenomas, lipomas, and uterine leiomyomas - what do they tell us?. Chromosome 12 Aberrations in Human Solid Tumors. Cytogenetics and Molecular Genetics. 1994; 46-52.
  394. Knight JC, Renwick P, Reeves B, Cotter F, Dal Cin P, Kempski H, Sonobe H, Fletcher C.D.M. Two categories of synovial sarcoma defined by t(X;18) breakpoints on chromosome Xp. 4th European Workshop on Cytogenetics and Molecular Genetics of Human Solid tumors. Cancer Genet Cytogenet. 1994; (77):161.
  395. Dal Cin P, Van den Berghe H . Cytogenetics of tumors of the female reproductive tract. . Repro Med Rev. 1994; 3:1-10.
  396. Schoenmakers EFPM, Kazmierczak B, Kools PFJ, Mols R, Dal Cin P, Bullerdiek J, Van den Berghe H, Van de Ven WJM. . Development and characterization of cell lines from a myxoid liposarcoma with t(12;16)(q13;p11.2) and trisomy 8. Chromosome 12 Aberrations in Human Solid Tumors. Cytogenetics and Molecular Genetics. 1994; 138-51.
  397. Dal Cin P, Sciot R, Fossion E, Van Damme B, Van den Berghe H. Chromosome abnormalities in cementifying fibroma. Cancer Genet Cytogenet. 1993 Dec; 71(2):170-2.
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  398. Dal Cin P, Trent JM. What should oncologists know about cytogenetics in solid tumors? Ann Oncol. 1993 Dec; 4(10):821-4.
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  399. Dal Cin P, Sciot R, Aly MS, Stas M, De Wever I, Van Damme B, Van den Berghe H. . Some desmoid tumors are characterized by trisomy 8. Human Genome Mapping Workshop 93 (HGM 93). 1993; Kobe, Japan.
  400. Sciot R, Dal Cin P, De Vos R, Van Damme B, De Wever I, Van den Berghe H, Desmet VJ. Alveolar soft-part sarcoma: evidence for its myogenic origin and for the involvement of 17q25. Histopathology. 1993 Nov; 23(5):439-44.
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  401. Dal Cin P, Kools P, De Jonge I, Moerman P, Van de Ven W, Van den Berghe H. Rearrangement of 12q14-15 in pulmonary chondroid hamartoma. Genes Chromosomes Cancer. 1993 Oct; 8(2):131-3.
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  402. Cuneo A, Demuynck H, Ferrant A, Louwagie A, Doyen C, Stul M, Cassiman JJ, Dal Cin P, Carli MG, Boogaerts M, Michaux, JL, Castolde GL, Van den Berghe H. Correlation of cytoimmunological features, cytogenetic patterns and clinical outcome in Ph-positive acute leukemia. XIIth Meeting of the International Society of Haematology. 1993; Vienna, Austria..
  403. Dal Cin P. Bone Tumours. Genetic aspects. International Symposium Reconstruction of the Upper Limb. 1993; Leuven, Belgium.
  404. Dal Cin P, Kools P, Sciot R, De Wever I, Van Damme B, Van de Ven W, Van den Berghe H. Cytogenetic and fluorescence in situ hybridization investigation of ring chromosomes characterizing a specific pathologic subgroup of adipose tissue tumors. Cancer Genet Cytogenet. 1993 Jul 15; 68(2):85-90.
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  405. Vanni R, Dal Cin P, Marras S, Moerman P, Andria M, Valdes E, Deprest J, Van den Berghe H. Endometrial polyp: another benign tumor characterized by 12q13-q15 changes. Cancer Genet Cytogenet. 1993 Jul 1; 68(1):32-3.
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  406. Aly MS, Dal Cin P, Jiskoot P, Deneffe G, Van den Berghe H. Competitive in situ hybridization in a mediastinal germ cell tumor. European Society of Human Genetics 25th Annual Meeting. 1993; Barcelona, Spain.
  407. Dal Cin P, De Wolf-Peeters C, Aly MS, Deneffe G, Van Mieghem W, Van Den Berghe H. Ring chromosome 6 as the only change in a thymoma. Genes Chromosomes Cancer. 1993 Apr; 6(4):243-4.
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  408. Dal Cin P. Significance of trisomy 7 and trisomy 10 in kidney tumors and surrounding arenchyma. . Southern African Society of Human Genetics, 5th Congress. 1993; South Africa .
  409. Dal Cin P. Cytogenetic investigations in endometrial polyps. Southern African Society of Human Genetics, 5th Congress. 1993; South Africa .
  410. Dal Cin P. Loss of the Y-chromosome in a malignant Sertoli tumor. Southern African Society of Human Genetics, 5th Congress. 1993; South Africa.
  411. Dal Cin P. ; . Chromosomes in solid tumors. 1993; South Africa .
  412. Dal Cin P. Trisomy 7 and trisomy 10 characterize subpopulations of tumor-infiltrating lymphocytes in kidney tumors and in the surrounding kidney tissue. 1993; South Africa.
  413. Dal Cin P. Chromosomes changes in pediatric tumors. 1993; South Africa.
  414. Johannisson E, Brosens I, Dal Cin P. The effect of ecapeptyl on the growht of leiomyomata. 3rd International Symposium on GnRH Analogues in Cancer and Human Redproduction. 1993.
  415. Aly MS, Dal Cin P, Moerman P, De Wever I, Devriendt K, Brock P, Casteels-Van Daele M, Van den Berghe H. Loss of the Y-chromosome in a malignant Sertoli tumor. Cancer Genet Cytogenet. 1993 Feb; 65(2):104-6.
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  416. Vanni R, Marras S, Moerman P, Andria M, Valdes E, Deprest L, Van den Berghe H, Dal Cin P. . Endometrial polyp. another benign tumor characterized by 12q14-15 changes ? 5th. International Workshop on Chromosomes in solid Tumors. 1993.
  417. Cuneo A, Ferrant A, Michaux JL, Boogaerts M, Demuynck H, Bosly A, Doyen CM, Carli MG, Piva N, Castoldi G, Stul M, Dal Cin P, Cassiman JJ, Van den Berghe H. Clinical review on features and cytogenetic patterns in adult acute myeloid leukemia with lymphoid markers. Leuk Lymph. 1993; 9:285-91.
  418. Dal Cin P, Van den Berghe H. The 6p21 chromosome region is non randomly involved in endometrial polyps. First International Workshop on Chromosome 6. Cytogenet Cell Genet. 1993; (62):82.
  419. Aly MS, Dal Cin P, Moerman P, De Wever I, Devriendt K, Brock P, Casteels-Van Damme M, Van den Berghe H. . Loss of the Y-chromosome in a malignant Sertoly tumor. 5th International Workshop on Chromosomes in solid Tumors. 1993.
  420. Dal Cin P, Puts JP, Gruwez J, De Wever I, Van Damme B, Van den Berghe H. Chromosomes changes in adipose tissue tumors. XIX international Congress of the International Academy of Pathology & 10th World Congress of Academic and Environmental Pathology. 1992.
  421. Dal Cin P, Aly MS, Delabie J, Ceuppens JL, Van Gool S, Van Damme B, Baert L, Van Poppel H, Van den Berghe H. Trisomy 7 and trisomy 10 characterize subpopulations of tumor-infiltrating lymphocytes in kidney tumors and in the surrounding kidney tissue. Proc Natl Acad Sci U S A. 1992 Oct 15; 89(20):9744-8.
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  422. Uyttebroeck A, De Groote B, Renard M, Brock P, Dal Cin P, Van den Berghe H, Casteels-Van Daele M. The occurrence of 5q- syndrome in a child. International Society of Paediatric Oncology (SIOP) XXIVth Meeting. 1992.
  423. Dal Cin P, Aly MS, De Wever I, Moerman P, Van Den Berghe H. Endometrial stromal sarcoma t(7;17)(p15-21;q12-21) is a nonrandom chromosome change. Cancer Genet Cytogenet. 1992 Oct 1; 63(1):43-6.
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  424. Dal Cin P, De Wolf F, Klerckx P, Van Den Berghe H. The 6p21 chromosome region is nonrandomly involved in endometrial polyps. Gynecol Oncol. 1992 Sep; 46(3):393-6.
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  425. Dal Cin P, Van Damme B, Hoogmartens M, Van Den Berghe H. Chromosome changes in a case of hibernoma. Genes Chromosomes Cancer. 1992 Sep; 5(2):178-80.
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  426. Van Poppel H, Dal Cin P, Aly MS, Delabie J, Ceuppens J, Van Damme B, Baert L, Van den Berghe H. . Cytogenetic investigations in normal and malignant kidney tissues. Euro-American Conference on Urological Cancer. 1992.
  427. Cuneo A, Carli MG, Piva N, Faglioli F, Pazzi I, Tallarico A, Ferrari L, Wlodarska I, Aly MS, Dal Cin P, Cassiman JJ, Van den Berghe H, Castoldi, G.L. Fluorescent in situ hybridization for the detection and monitoring of trisomy 12 in B-cell chronic lymphocytic leukaemia. FISH Meeting. 1992.
  428. Dal Cin P, Rao U, Jani-Sait S, Karakousis C, Sandberg AA. Chromosomes in the diagnosis of soft tissue tumors. I. Synovial sarcoma. Mod Pathol. 1992 Jul; 5(4):357-62.
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  429. Dal Cin P, Sneyers W, Aly MS, Segers A, Ostijn F, Van Damme B, Van Den Berghe H. Involvement of 19q13 in follicular thyroid adenoma. Cancer Genet Cytogenet. 1992 May; 60(1):99-101.
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  430. Dal Cin P, Moerman P, De Wever I, Van den Berghe H. Numerical chromosome aberrations in fibrothecoma. Tumori. 1992 Apr 30; 78(2):140-2.
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  431. Van Roy N, Laureys G, Benoit Y, Heyman P, Sariban E, Caron H, Dal Cin P, Brock P.R., Speleman F. Molecular cytogenetic detection of chromosome 1 abnormalities and MYCN amplification in neuroblastoma interphase nuclei. Third European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. Cancer Genet Cytogenet. 1992; (63):167.
  432. Schoenmakers E, Mols R, Willems M, Dal Cin P, Bullerdiek J, Van Den Berghe H, Van de Ven W. . Strategy to maP YAC-derived sequence tagged sites in human chromosome region 12q13-15 using the newly developed hybrid cell line LIS-3/SV40/A9-B4. International Workshop on Cytogenetics and Molecular Genetics of Chromosome 12 in Human Solid Tumors. 1992.
  433. Gole L, Kazmierczak B, Jox A, Dal Cin P, Bullerdiek J, Bartnitzke S. . Malignant tumors from cell lines derived from tumors with 12q13-15 aberrations. International Workshop on Cytogenetics and Molecular Genetics of Chromosome 12 in Human Solid Tumors. 1992.
  434. Kazmierczak B, Belge G, Stern C, Dal Cin P, Van den Berghe H, Bartnitzke S, Bullerdiek J. Cell lines from human tumors showing the 12q13-15 aberrations. International Workshop on Cytogenetics and Molecular Genetics of Chromosome 12 in Human Solid Tumors. 1992.
  435. Cuneo A, Michaux JL, Ferrant A, Van Hove L, Bosly A, Stul M, Dal Cin P, Vandenberghe E, Cassiman JJ, Negrini M, et al. Correlation of cytogenetic patterns and clinicobiological features in adult acute myeloid leukemia expressing lymphoid markers. Blood. 1992 Feb 1; 79(3):720-7.
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  436. Foschini MP, Van Eyken P, Brock PR, Casteels-Van Daele M, De Vos R, Dal Cin P, Van den Berghe H, Desmet VJ. Malignant rhabdoid tumour of the liver. A case report. Histopathology. 1992 Feb; 20(2):157-65.
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  437. Aly MS, Dal Cin P, De Wever I, Moerman PH, Van den Berghe H. Endometrial stromal sarcoma. t(7;17)(p15-21;q12-21) is a non-random chromosome change. Third European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. Cancer Genet Cytogenet. 1992; (63):132.
  438. Dal Cin P, Aly MS, De Wever I, Van Damme B, Van den Berghe H . Does chromosome investigation discriminate between benign and malignant gastrointestinal leiomyomatous tumors?. Diag Oncol. 1992; 2:55-59.
  439. Cuneo A, Castoldi G, Michaux JL, Ferrant A, Bosly A, Boogaerts M, Dal Cin P, Van den Berghe H. Adult acute myeloid leukemia. Adult acute myeloid leukemia. Blood. 1992; 80:1369-70.
  440. Dal Cin P, De Wolf F, Klerckx P, Van Den Berghe H. The 6p21 chromosome region is non randomly involved in endometrial polyps.Eighty-third Annual Meeting of the American Association for Cancer Research. Proceedings of the American Association for Cancer Research. 1992; (33):398.
  441. Hilliker C, Delabie J, Bilbe G, Brüggen J, Speleman F, Dal Cin P, Van Leuven F, Van Den Berghe H. Localization of an intermediate filament associated protein expressed in the Reed-Sternberg cell to 12q24.1-q24.33. Eighty-third Annual Meeting of the American Association for Cancer Research. Proceedings of the American Association for Cancer Research. 1992; (33):398.
  442. Rege-Cambrin G, Speleman F, Kerim S, Scaravaglio P, Carozzi F, Dal Cin P, Michaux JL, Offner F, Saglio G, Van den Berghe H. Extra translocation +der(1q9p) is a prognostic indicator in myeloproliferative disorders. Leukemia. 1991 Dec; 5(12):1059-63.
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  443. Dal Cin P. . Cytogenetics in the diagnosis of soft tumors. Eur J Cancer suppl. 1991; (27):S5.
  444. Dal Cin P, van Gool S, Brock P, Proesmans W, Casteels-van Daele M, de Wever I, Baert L, van Damme B, van den Berghe H. Renal cell carcinoma in a child. Cancer Genet Cytogenet. 1991 Nov; 57(1):137-8.
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  445. Meltzer PS, Jankowski SA, Dal Cin P, Sandberg AA, Paz IB, Coccia MA. Identification and cloning of a novel amplified DNA sequence in human malignant fibrous histiocytoma derived from a region of chromosome 12 frequently rearranged in soft tissue tumors. Cell Growth Differ. 1991 Oct; 2(10):495-501.
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  446. Dal Cin P, Brock P, Aly MS, Casteels-Van Daele M, De Wever I, Van Damme B, Van den Berghe H. A variant (2;13) translocation in rhabdomyosarcoma. Cancer Genet Cytogenet. 1991 Sep; 55(2):191-5.
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  447. Dal Cin P, De Wever I, Moerman P, Van den Berghe H. Translocation X;12 in mesothelioma. Cancer Genet Cytogenet. 1991 Aug; 55(1):115-8.
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  448. Stern C, Kazmierczak B, Thode B, Rommel B, Bartnitzke S, Dal Cin P, van de Ven W, Van den Berghe H, Bullerdiek J. Leiomyoma cells with 12q15 aberrations can be transformed in vitro and show a relatively stable karyotype during precrisis period. Cancer Genet Cytogenet. 1991 Jul 15; 54(2):223-8.
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  449. Aly MS, Dal Cin P, Van Poppel H, Baert L, Van Damme B, Cassiman JJ, Van den Berghe H. Cytogenetic investigations in normal and malignant kidney tissues. European Society of Human Genetics Annual Meeting. 1991.
  450. Speleman F, Dal Cin P, Van Roy N, Van Marck E, Buytaert P, Van den Berghe H, Leroy JG. Is t(6;20)(p21;q13) a characteristic chromosome change in endometrial polyps? Genes Chromosomes Cancer. 1991 Jul; 3(4):318-9.
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  451. Dal Cin P, Brock P, Casteels-Van Daele M, De Wever I, Van Damme B, Van den Berghe H. Cytogenetic characterization of congenital or infantile fibrosarcoma. Eur J Pediatr. 1991 Jun; 150(8):579-81.
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  452. Cuneo A, Gretel Carli M, Piva N, Fagioli F, Vandenberghe E, Dal Cin P, Castoldi G, Van Den Berghe H. Clinicopathological evolution and multilineage involvement in erythroleukemia: report of a case. Haematologica. 1991 May-Jun; 76(3):235-7.
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  453. Dal Cin P, De Wever I, Aerts R, Van Damme B, Van den Berghe H. Trisomy 8 as the only chromosome change in an epithelioid smooth muscle tumor. Genes Chromosomes Cancer. 1991 May; 3(3):235-7.
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  454. Dal Cin P, Van Den Berghe H, Brosens I. Involvement of 6p in an endometrial polyp. Cancer Genet Cytogenet. 1991 Feb; 51(2):279-80.
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  455. Rege-Cambrin G, Scaravaglio P, Carozzi F, Saglio G, Speleman F, Dal Cin P, Van den Berghe H. Traslocazione t(1q;9p) in associazione con la trasformazione acuta di syndromi mieloproliferative. 33„a Congresso Societa' Italiana di Ematologia. 1991.
  456. Corallini A, Gianni M, Mantovani C, Vandini A, Rimessi P, Negrini M, Giavazzi R, Bani MR, Milanesi G, Dal Cin P, Van den Berghe H, Barbanti-Brodano G. . Transformation of human cells by recombinant DNA molecules containing BK virus early region and the human activated c-H-ras or c-myc oncogenes. Cancer J. 1991; 4:24-34.
  457. Groupe Français de Cytogénétique Hématologique. Isochromosome 21q in hematologic malignancies. Cancer Genet Cytogenet. 1991; 55:101-105.
  458. Dal Cin P, Speleman F, Van Roy N, Van Marck E, Buytaert P, Van den Berghe H. . Is t(6;20)(p21;q13) a characteristic chromosome change in endometrial polyp?. 4th International Workshop on Chromosomes in Solid Tumors.Cancer Genet Cytogenet. 1991; (56):85.
  459. Speleman F, Mangelschots K, Vercruyssen M, Dal Cin P, Aventin A, Offner F, Laureys G, Van den Berghe H, Leroy J. Analysis of whole-arm translocations in malignant blood cells by nonisotopic in situ hybridization. Cytogenet Cell Genet. 1991; 56(1):14-7.
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  460. van den Berghe E, de Wolf-Peeters C, Louwagie A, Thomas J, Wlodarska I, Dal Cin P, Stul M, Cassiman JJ, Mecucci C, van den Berghe H. Chromosome 1p abnormalities in B non Hodgkin's lymphoma. Leuk Lymphoma. 1991; 5(2-3):193-9.
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  461. Van den Berghe E, De Wolf-Peeters C, Louwagie A, Thomas J, Wlodarska I, Dal Cin P, Stul M, Cassiman JJ, Mecucci C, Van den Berghe H. Chromosome 1p abnormalities in B non-Hodgkin lymphoma. Leukemia and Lymphoma. 1991; 5:193-1999.
  462. Meltzer PS, Jankowski SA, Dal Cin P, Sandberg AA, Paz IB, Coccia MA, Smith SH. Identification and cloning of a novel amplified DNA sequence in human malignant fibrous histiocytoma derived from a region of chromosome 12 frequently rearranged in soft tissue tumors. Human Gene Mapping 11. Cytogenet Cell Genet. 1991; (58):1979.
  463. Dal Cin P, Rege-Cambrin G, Speleman F, Van Roy N, Kerim S, Scaravaglio P, Carozzi F, Michaux JL, Offner F, Saglio G, Van den Berghe H. More precize localization of breakpoints involved in the derivative chromosome (1q9p), associated with myeloproliferative disorders. Human Gene Mapping 11. Cytogenet Cell Genet. 1991; (58):1852.
  464. Cuneo A, Michaux JL, Ferrand A, Bosly A, Van Hove L, Dal Cin P, Piva N, Fagioli F, Carli MG, Castoldi GL, Van den Berghe H. Cytogenetic and biomolecular studies in acute myeloid leukemia (AML) with lymphoid markers. 20th Annual ISEH Meeting. 1991.
  465. Dal Cin P, Van den Berghe H. Isochromosome (12p) in germ cell tumors. Recent Results Cancer Res. 1991; 123:107-11.
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  466. Dal Cin P, Van den Berghe H. . i(12p) in germ cell tumors. Pathobiology of Human Germ Cell Neoplasia. 1991; 123:107-111.
  467. 1Van Gool S, Brock P, Proesmans W, Dal Cin P, Van den Berghe H, Van Damme B, De Wever I, Baert L, Casteels-Van Daele M. Renal cell carcinoma in a child. International Society of Paediatric Oncology (SIOP) XXIIIrd Meeting. Med & Pediatr Oncol. 1991; (19):392.
  468. Renard M, Brock P, Kruger M, De Wever I, Smet M, Vandamme B, Dal Cin P, Casteels-Van Daele M. Chemotherapy in congenital fibrosarcoma. International Society of Paediatric Oncology (SIOP) XXIIIrd Meeting. Med & Pediatr Oncol. 1991; (19):362.
  469. Paulien S, Turc-Carel C, Dal Cin P, Jani-Sait S, Sreekantaiah C, Leong SP, Vogelstein B, Kinzler KW, Sandberg AA, Gemmill RM. Myxoid liposarcoma with t(12;16) (q13;p11) contains site-specific differences in methylation patterns surrounding a zinc-finger gene mapped to the breakpoint region on chromosome 12. Cancer Res. 1990 Dec 15; 50(24):7902-7.
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  470. Dal Cin P, Johanisson E, Brosens I. Cytogenetic analysis of leiomyoma in relation to GnRH agonist treatment. 2nd International Symposium on GnRH Analogues in Cancer and Human Reproduction. 1990.
  471. Vanni R, Dal Cin P, Van Den Berghe H. Is the chromosome band 1p36 another hot-spot for rearrangements in uterine leiomyoma? Genes Chromosomes Cancer. 1990 Sep; 2(3):255-6.
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  472. Cuneo A, Van Orshoven A, Michaux JL, Boogaerts M, Louwagie A, Doyen C, Dal Cin P, Fagioli F, Castoldi G, Van den Berghe H. Morphologic, immunologic and cytogenetic studies in erythroleukaemia: evidence for multilineage involvement and identification of two distinct cytogenetic-clinicopathological types. Br J Haematol. 1990 Jul; 75(3):346-54.
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  473. Speleman F, Mangelschots K, Vercruyssen M, Dal Cin P, Aventin A, Offner F, Laureys G, Leroy J, Van den Berghe H. Analysis of whole-arm translocations in malignant hematologic cells by non-isotopic in situ hybridization. European Society of Human Genetics Symposium. 1990.
  474. Kerim S, Stul M, Mecucci C, Vandenberghe E, Cuneo A, Dal Cin P, Michaux JL, Louwagie A, Cassiman JJ, Van den Berghe H. Rearrangement of immunoglobulin and TCR genes in lymphoid blast crisis of Ph+ chronic myeloid leukaemia. Br J Haematol. 1990 Apr; 74(4):414-9.
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  475. Speleman F, De Potter C, Dal Cin P, Mangelschots K, Ingelaere H, Laureys G, Benoit Y, Leroy J, Van Den Berghe H. i(12p) in a malignant ovarian tumor. Cancer Genet Cytogenet. 1990 Mar; 45(1):49-53.
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  476. Dal Cin P, Sandberg AA. Karyotypic analysis of solid tumors. Curr Top Pathol. 1990; 82:257-88.
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  477. Dal Cin P, Sandberg AA. Karyotypic analysis of solid tumors. J.C.E. Underwood, Ed. Current Topics in Pathology: Pathology of the Nucleus. 1990.
  478. Fourth MIC Cooperative Study Group. Meeting Report. Morphologic, immunologic, and cytogenetic classification of the chronic (mature) B and T lymphoid leukemias. Cancer Res. 1990; 2212.
  479. Speleman F, Mannens M, Laureys G, Cuvelier C., Dal Cin P, Benoit Y, Leroy JG. Cytogenetic and molecular studies in a case of mesoblastic nephroma. European Workshop on Cytogenetics and Molecular Genetics in Human Solid Tumors. 1990.
  480. Coccia M, Meltzer P, Dal Cin P, Turc-Carel C, Sandberg AA, Trent J. . A recurring DNA amplification in human sarcomas. American Association for Cancer Research. 1990.
  481. Paulien S, Turc-Carel C, Dal Cin P, Sandberg AA, Gemmill R. Mapping studies aroudn the 12q13-q14 region in adipose tissue tumors. Second European Workshop on Cytogenetics and Molecular Genetics in Human Solid Tumors. 1990.
  482. Dal Cin P, Drochmans A, Moerman PH, Van den Berghe H. Isochromosome 12p in a mediastinal germ cell tumor. Genetics in Cancer & Development. Clin. Genet. 1990; (37):300.
  483. Fourth MIC Cooperative Study Group. Meeting Report. A Conference on the Morphologic, Immunologic, and Cytogenetic Classification of the Chronic (mature) B and T Lymphoid Leukaemias. Cancer Genet Cytogenet. 1990; 131-132.
  484. Hashimura T, Tubbs RR, Connelly R, Caulfield MJ, Trindade CS, McMahon JT, Galetti TP, Edinger M, Sandberg AA, Dal Cin P, et al. Characterization of two cell lines with distinct phenotypes and genotypes established from a patient with renal cell carcinoma. Cancer Res. 1989 Dec 15; 49(24 Pt 1):7064-71.
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  485. Boghosian L, Dal Cin P, Turc-Carel C, Rao U, Karakousis C, Sait SJ, Sandberg AA. Three possible cytogenetic subgroups of leiomyosarcoma. Cancer Genet Cytogenet. 1989 Nov; 43(1):39-49.
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  486. Dal Cin P, Drochmans A, Moerman P, Van den Berghe H. Isochromosome 12p in mediastinal germ cell tumor. Cancer Genet Cytogenet. 1989 Oct 15; 42(2):243-51.
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  487. Cuneo A, Kerim S, Vandenberghe E, Van Orshoven A, Rodhain J, Bosly A, Zachee P, Louwagie A, Michaux JL, Dal Cin P, et al. Translocation t(6;9) occurring in acute myelofibrosis, myelodysplastic syndrome, and acute nonlymphocytic leukemia suggests multipotent stem cell involvement. Cancer Genet Cytogenet. 1989 Oct 15; 42(2):209-19.
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  488. Cuneo A, Mecucci C, Kerim S, Vandenberghe E, Dal Cin P, Van Orshoven A, Rodhain J, Bosly A, Michaux JL, Martiat P, et al. Multipotent stem cell involvement in megakaryoblastic leukemia: cytologic and cytogenetic evidence in 15 patients. Blood. 1989 Oct; 74(5):1781-90.
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  489. Dal Cin P, Gaeta J, Huben R, Li FP, Prout GR, Sandberg AA. Renal cortical tumors. Cytogenetic characterization. Am J Clin Pathol. 1989 Oct; 92(4):408-14.
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  490. Dal Cin P, Van den Berghe H. . Cytogenetic analysis on uterine leiomyomas. Voordrachten "Myomatosis", Vlaamse Vereniging voor Obstetrie en Gynaecologie. 1989.
  491. Speleman F, De Telder V, De Potter KR, Dal Cin P, Van Daele S, Benoit Y, Leroy JG, Van den Berghe H. Cytogenetic analysis of a mesenchymal hamartoma of the liver. Cancer Genet Cytogenet. 1989 Jul 1; 40(1):29-32.
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  492. Dal Cin P, Turc Carel C, Sandberg AA, Van den Berghe H. More precise localization of GLI gene by in situ hybridization. Human Genet Mapping 10. 1989.
  493. Speleman F, Dal Cin P, De Potter K, Laureys G, Roels HJ, Leroy J, Van Den Berghe H. Cytogenetic investigation of a case of congenital fibrosarcoma. Cancer Genet Cytogenet. 1989 May; 39(1):21-4.
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  494. Coccia M, Meltzer P, Dal Cin P, Turc Carel C, Sait S, Sandberg AA, Trent J. . DNA sequence amplification in malignant fibrous histiocytoma. 80th Annual Meeting, American Association for Cancer Research. 1989.
  495. Speleman F, De Potter C, Dal Cin P, Mangelschots K, Laureys G, Leroy JG, Van den Berghe H. i(12p) in a malignant ovarian tumor. Genetics in Cancer & Development. 1989.
  496. Coccia M, Meltzer P, Dal Cin P, Turc Carel C, Sait S, Sandberg AA. . DNA sequence amplification in malignant fibrous histiocytoma tumors. 3rd International Workshop on Chromosomes in Solid Tumors. 1989.
  497. Pauline S, Sait S, Dal Cin P, Turc Carel C, Leong SPL, Sandberg AA, Vogelstein B, Gemmill RM. Tissie specific pulsed field gel fragment patterns in a 700 KB domain surrounding GLI. 3rd International Workshop on Chromosomes in Solid Tumors. 1989.
  498. Sait SN, Dal Cin P, Sandberg AA, Leong S, Karakousis C, Rao U, Harris K. Involvement of 6p in benign lipomas. A new cytogenetic entity? Cancer Genet Cytogenet. 1989 Feb; 37(2):281-3.
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  499. Sait SN, Dal Cin P, Ovanessoff S, Sandberg AA. A uterine leiomyoma showing both t(12;14) and del(7) abnormalities. Cancer Genet Cytogenet. 1989 Feb; 37(2):157-61.
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  500. Dal Cin P, Sandberg AA. Chromosome changes in soft tissue tumors: benign and malignant. Cancer Invest. 1989; 7(1):63-76.
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  501. Dal Cin P, Sandberg AA. Chromosomal aspects of human oncogenesis. Crit Rev Oncog. 1989; 1(2):113-26.
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  502. Van den Berghe H, Dal Cin P. Some aspects of chromosomes and oncogenes in hematologic malignancies. Biol Clin Hematológia. 1989; 11:45 -51.
  503. Turc-Carel C, Dal Cin P, Boghosian L, Leong SP, Sandberg AA. Breakpoints in benign lipoma may be at 12q13 or 12q14. Cancer Genet Cytogenet. 1988 Nov; 36(1):131-5.
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  504. Dal Cin P, Talcott J, Abrams J, Li FP, Sandberg AA. Ins(10;19) in an endometrial stromal sarcoma. Cancer Genet Cytogenet. 1988 Nov; 36(1):1-5.
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  505. Dal Cin P, Li FP, Prout GR, Huben RP, Limon J, Ferti-Passantonopoulou A, Richie JP, Sandberg AA. Involvement of chromosomes 3 and 5 in renal cell carcinoma. Cancer Genet Cytogenet. 1988 Oct 1; 35(1):41-6.
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  506. Sait SN, Dal Cin P, Sandberg AA. Consistent chromosome changes in leiomyosarcoma. Cancer Genet Cytogenet. 1988 Oct 1; 35(1):47-50.
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  507. Boghosian L, Dal Cin P, Sandberg AA. An interstitial deletion of chromosome 7 may characterize a subgroup of uterine leiomyoma. Cancer Genet Cytogenet. 1988 Sep; 34(2):207-8.
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  508. Kakati S, Limon J, Dal Cin P, Pietrzak E, Kinniburgh AJ, Li FP, Sandberg AA. Abnormally banded region in a poorly differentiated sarcoma is not correlated with amplification of c-MYC or c-MOS protooncogenes. Cancer Genet Cytogenet. 1988 Aug; 34(1):111-5.
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  509. Dal Cin P, Boghosian L, Crickard K, Sandberg AA. t(10;17) as the sole chromosome change in a uterine leiomyosarcoma. Cancer Genet Cytogenet. 1988 Jun; 32(2):263-6.
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  510. Dal Cin P, Sandberg AA, Huben R, Li FP, Prout GR. New cytogenetic subtype of renal tumors. Cancer Genet Cytogenet. 1988 Jun; 32(2):313.
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  511. Turc-Carel C, Dal Cin P, Boghosian L, Terk-Zakarian J, Sandberg AA. Consistent breakpoints in region 14q22-q24 in uterine leiomyoma. Cancer Genet Cytogenet. 1988 May; 32(1):25-31.
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  512. Huben RP, Dal Cin P, Prout Jr. GR, Li P, Sandberg AA. . Recurrent karyotype in renal cell carcinoma/cortical adenoma. Annual Meeting of American Urological Society. 1988.
  513. Dal Cin P, Turc-Carel C, Sandberg AA. Consistent involvement of band 12q14 in two different translocations in three lipomas from the same patient. Cancer Genet Cytogenet. 1988 Apr; 31(2):237-40.
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  514. Fan YS, Rowe JM, Dal Cin PD, Sandberg AA. A translocation t(9;11)(p11;q23) in T-cell acute lymphoblastic leukemia (FAB-l2). Cancer Genet Cytogenet. 1988 Apr; 31(2):263-9.
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  515. Psihramis KE, Dal Cin P, Dretler SP, Prout GR, Sandberg AA. Further evidence that renal oncocytoma has malignant potential. J Urol. 1988 Mar; 139(3):585-7.
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  516. Turc-Carel C, Dal Cin P, Carr K, Sandberg AA. Normal blood lymphocytes from patients with adipose tissue tumors with rearrangements at 12q13-q14 do not express the fragile site fra(12)(q13.1). Cancer Genet Cytogenet. 1988 Mar; 31(1):35-9.
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  517. Dal Cin P, Boghosian L, Sandberg AA. Chromosome changes in a prostatic leiomyosarcoma. Cancer Genet Cytogenet. 1988 Feb; 30(2):339-40.
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  518. Dal Cin P, Sandberg AA. Cytogenetic findings in a supratentorial ependymoma. Cancer Genet Cytogenet. 1988 Feb; 30(2):289-93.
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  519. Dal Cin P, Boghosian L, Sandberg AA. Cytogenetic findings in leiomyosarcoma of the small bowel. Cancer Genet Cytogenet. 1988 Feb; 30(2):285-8.
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  520. Limon J, Dal Cin P, Sait SN, Karakousis C, Sandberg AA. Chromosome changes in metastatic human melanoma. Cancer Genet Cytogenet. 1988 Feb; 30(2):201-11.
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  521. Dal Cin P, Rao U, Turc-Carel C, Sandberg AA. Translocation (7;21) in a lipoma. Cancer Genet Cytogenet. 1988 Jan; 30(1):17-22.
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  522. Turc-Carel C, Dal Cin P, Rao U, Karakousis C, Sandberg AA. Recurrent breakpoints at 9q31 and 22q12.2 in extraskeletal myxoid chondrosarcoma. Cancer Genet Cytogenet. 1988 Jan; 30(1):145-50.
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  523. Dal Cin P, Sandberg AA. Cytogenetic abnormalities and human cancer. ISI Atlas Science. Biochem. 1988; (1):273-78.
  524. Fan YS, Baer MR, Sait SN, Dal Cin P, Prentice TC, Preisler HD, Sandberg AA. An acquired Robertsonian translocation dic(14;14)(p11;p11) in a patient with a myelodysplastic syndrome following treatment of multiple myeloma. Cancer Genet Cytogenet. 1988 Jan; 30(1):133-7.
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  525. Karakousis CP, Dal Cin P, Turc-Carel C, Limon J, Sandberg AA. Chromosomal changes in soft-tissue sarcomas. A new diagnostic parameter. Arch Surg. 1987 Nov; 122(11):1257-60.
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  526. Limon J, Dal Cin P, Gaeta J, Sandberg AA. Translocation t(4;11)(q35;p13) in an adrenocortical carcinoma. Cancer Genet Cytogenet. 1987 Oct; 28(2):343-8.
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  527. Kakati S, Limon J, Dal Cin P, Pietrzak E, Kinniburgh J, Sandberg AA. . A homogeneously stain region on chromosome 8 in an osteosarcoma without amplification of MYC and MOS oncogenes. American Society of Human Genetics. 1987.
  528. Turc Carel C, Dal Cin P, Sandberg AA. . Breakpoints 9q22 q31 and 22q12 are associated with extraskeletal myxoid chondrosarcoma. Human Gene Mapping 9. 1987.
  529. Dal Cin P, Turc Carel C, Limon J, Leong S, Sandberg AA. . Consistent involvement of band 12q14 in benign lipoma. Human Gene Mapping 9. 1987.
  530. Limon J, Dal Cin P, Kakati S, Huben RP, Sandberg AA. Cytogenetic findings in a primary adrenocortical carcinoma. Cancer Genet Cytogenet. 1987 Jun; 26(2):271-7.
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  531. Sait SN, Dal Cin P, Sandberg AA. Recurrent involvement of 11q13 in acute nonlymphocytic leukemia. Cancer Genet Cytogenet. 1987 Jun; 26(2):351-4.
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  532. Turc-Carel C, Dal Cin P, Sandberg AA. Nonrandom translocation in extraskeletal myxoid chondrosarcoma. Cancer Genet Cytogenet. 1987 Jun; 26(2):377.
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  533. Turc-Carel C, Dal Cin P, Limon J, Rao U, Li FP, Corson JM, Zimmerman R, Parry DM, Cowan JM, Sandberg AA. Involvement of chromosome X in primary cytogenetic change in human neoplasia: nonrandom translocation in synovial sarcoma. Proc Natl Acad Sci U S A. 1987 Apr; 84(7):1981-5.
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  534. Karakousis CP, Dal Cin P, Turc Carel C, Limon J, Sandberg AA. . Chromosome changes in sarcomas. A new diagnostic parameter. Annual Meeting of the Society of Surgical Oncology. 1987.
  535. Dal Cin P, Turc Carel C, Limon J, Parry DM, Li FP, Sandberg AA. Reciprocal translocations involving Xp11.2 and 18q11.2 in soft tissue sarcomas. Cancer Genet Cytogenet. 1987; (28):40.
  536. Huben RP, Dal Cin P, Limon J, Yoshida M, Sandberg AA. Cytogenetic definition of kidney tumors. J Urol. 1987; (137):252A.
  537. Turc Carel C, Dal Cin P, Limon J, Gibas Z, Kakati S, Pietrzak E, Parry D, Li F, Sandberg AA. Cytogenetic and molecular studies of adipose tissue tumors. Cancer Genet Cytogenet. 1987; (28):33.
  538. Trindade CS, Connelly R, Hashimura T, Sandberg AA, Dal Cin P, Tubbs R. Establishment of two new renal cell carcinoma lines. Biological difference of cells from the primary tumor versus those of renal vein effluent. J Urol. 1987; (137):252A.
  539. Gibas Z, Limon J, Li FP, Karakousis C, Dal Cin P, Parry D, Sandberg AA. . Chromosomal rearrangements in soft tissue sarcomas. Cancer Genet Cytogenet. 1987; (28):33.
  540. Limon J, Dal Cin P, Sandberg AA. Application of long-term collagenase disaggregation for the cytogenetic analysis of human solid tumors. Cancer Genet Cytogenet. 1986 Dec; 23(4):305-13.
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  541. Turc-Carel C, Limon J, Dal Cin P, Rao U, Karakousis C, Sandberg AA. Cytogenetic studies of adipose tissue tumors. II. Recurrent reciprocal translocation t(12;16)(q13;p11) in myxoid liposarcomas. Cancer Genet Cytogenet. 1986 Dec; 23(4):291-9.
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  542. Turc-Carel C, Dal Cin P, Rao U, Karakousis C, Sandberg AA. Cytogenetic studies of adipose tissue tumors. I. A benign lipoma with reciprocal translocation t(3;12)(q28;q14). Cancer Genet Cytogenet. 1986 Dec; 23(4):283-9.
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  543. Limon J, Dal Cin P, Sandberg AA. Translocations involving the X chromosome in solid tumors: presentation of two sarcomas with t(X;18)(q13;p11). Cancer Genet Cytogenet. 1986 Sep; 23(1):87-91.
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  544. Turc-Carel C, Dal Cin P, Limon J, Li F, Sandberg AA. Translocation X;18 in synovial sarcoma. Cancer Genet Cytogenet. 1986 Sep; 23(1):93.
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  545. Jani Sait SN, Dal Cin P, Sandberg AA. t(Y;18) in acute myeloblastic leukemia FAB type M2. Cancer Genet Cytogenet. 1986 Aug; 22(4):367-8.
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  546. Limon J, Dal Cin P, Sandberg AA. Cytogenetic findings in a primary leiomyosarcoma of the prostate. Cancer Genet Cytogenet. 1986 Jun; 22(2):159-67.
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  547. Limon J, Turc-Carel C, Dal Cin P, Rao U, Sandberg AA. Recurrent chromosome translocations in liposarcoma. Cancer Genet Cytogenet. 1986 May; 22(1):93-4.
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  548. Limon J, Rao U, Dal Cin P, Gibas Z, Sandberg AA. Translocation (13;22) in a hemangiopericytoma. Cancer Genet Cytogenet. 1986 Apr 15; 21(4):309-18.
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  549. Gibas Z, Limon J, Dal Cin P, Karakousis C, Sandberg AA. Chromosomal rearrangements in soft tissue sarcoma. Am J Hum Genet (suppl). 1986; (A31):87.
  550. Turc Carel C, Limon J, Dal Cin P, Sandberg AA. . Recurrent chromosome rearrangements in malignant and benign adipose tissue tumors. J Cell Biochem (suppl). 1986; 10A:42.
  551. Dal Cin P, Turc Carel C, Carr K, Sandberg AA. . Is fragile site 12q13 involved in the genesis of adipose tissue tumors ?. Am J Hum Genet (suppl). 1986; (A28):77.
  552. Parry DM, Li F, Rosenberg SA, Turc Carel C, Dal Cin P, Limon J, Rao U, Sandberg AA. Rearrangements involving Xp and 18q in soft tissue sarcomas. Am J Hum Genet (suppl). 1986; (A37):104.
  553. Dal Cin P, Diaz MC, Vargas A, Sanoja A, Piras R, Piras MM. Analisis de resultados de 814 diagnosticos prenatales para alteraciones cromosomicas y defectos del tubo neural. (Analysis of 814 prenatal diagnoses for chromosomal aberrations and neural tube defects). Acta Cient Venez. 1983; 34:345.
  554. Dal Cin P, Diaz MC, Piras MM, Cohen R. . Diagnostico prenatal de agenesia del cuerpo callosos y de labio leporino en un feto portador de trisomia 5p. (Prenatal diagnosis of agenesis corpus callosum and cleft lip in a fetus carrier of trisomy 5p). Acta Cient Venez. 1983; 34:345.
  555. Dal Cin P, Piras MM. Experiencia de laboratoria en el manejo de liquidos amnioticos para del diagnostico prenatal de alteraciones cromosomicas y defectos del tubo neural. (Experience in management of amniotic fluids for diagnosis of chromosome aberrations in prenatal and neural tube defects). Acta Cient Venez. 1981; 32:299.
  556. Dal Cin P, Paolini P, Borberg C, Casanova J, Martinez P, Sanoja A, Bustamante A, Muro de D'Hoy E, Piras MM. . Diagnostico prenatal de alteraciones cromosomicas y de tubo neural. Experiencia recogida en cultivos de celulas amnioticas y en la determinacion de Ó fetoproteina. (prenatal diagnosis of chromosome aberrations and neural tube defects. Experience of amniotic fluid cell cultures and determination of fetoprotein.). Acta Cient Venez. 1980; 31:184.
  557. Paolini P, Dal Cin P, Nascimento J, Ponce C. . Dos casos de trisomia 9p con cariotipos diferentes. 47,XX,+9q y 46,XX,dic(9)(pter„_q32..p22„_cen„_qter). (Two cases with trisomy 9p with different karyotypes. 47,XX,+9q and 46,XX,dic(9) (pter„_q32:p22„_cen„_qter). Acta Cient Venez. 1980; 31:136.
  558. Paolini P, Dal Cin P, Segal J. Sobre un caso de triple X (A case of 47,XXX). Acta Cient Venez. 1980; 31:135.
  559. Piovan E, Dal Cin P, Goppion G, Tenconi R, Baccichetti C. Sister chromatid exchanges induced by bromodeoxyuridine and caffeine. Acta Med Auxol. 1977; 9:159.
  560. Takahashi H, Feuerhake F, Kutok J L, Monti S, Dal Cin P, Neuberg D, Aster J C, Shipp M A. . FAS death domain deletions and incereased c-Fliplong expression occur in different subtypes of diffuse large B-cell lymphoma. 1920.
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