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One or more keywords matched the following items that are connected to Slaugenhaupt, Susan
Item TypeName
Academic Article New locus for autosomal dominant mitral valve prolapse on chromosome 13: clinical insights from genetic studies.
Academic Article Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31.
Academic Article Targeted genome screen of panic disorder and anxiety disorder proneness using homology to murine QTL regions.
Academic Article Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17.
Academic Article Gene-centromere mapping and the study of non-disjunction in autosomal trisomies and ovarian teratomas.
Academic Article Isolation of a marker linked to the Charcot-Marie-Tooth disease type IA gene by differential Alu-PCR of human chromosome 17-retaining hybrids.
Academic Article A genetic linkage map of 27 markers on human chromosome 21.
Academic Article Linkage mapping of D21S171 to the distal long arm of human chromosome 21 using a polymorphic (AC)n dinucleotide repeat.
Academic Article A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10.
Academic Article Genetic linkage map of fishes of the genus Xiphophorus (Teleostei: Poeciliidae).
Academic Article Prenatal diagnosis of familial dysautonomia by analysis of linked CA-repeat polymorphisms on chromosome 9q31-q33.
Academic Article Linkage analysis of neurofibromatosis type I, using chromosome 17 DNA markers.
Academic Article Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome.
Academic Article The gene for achondroplasia maps to the telomeric region of chromosome 4p.
Academic Article Linkage mapping of highly informative DNA polymorphisms within the human interferon-alpha receptor gene on chromosome 21.
Academic Article A locus for autosomal dominant mitral valve prolapse on chromosome 11p15.4.
Academic Article Methods for studying recombination on chromosomes that undergo nondisjunction.
Academic Article Linkage analysis of the human HMG14 gene on chromosome 21 using a GT dinucleotide repeat as polymorphic marker.
Academic Article DNA duplication associated with Charcot-Marie-Tooth disease type 1A.
Academic Article Reduced recombination rate on chromosomes 21 that have undergone nondisjunction.
Academic Article An index marker map of chromosome 9 provides strong evidence for positive interference.
Academic Article Prenatal diagnostic testing for familial dysautonomia using linked genetic markers.
Academic Article The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms.
Academic Article Exclusion of familial dysautonomia from more than 60% of the genome.
Academic Article Evidence against close linkage of unipolar affective illness to human chromosome 11p markers HRAS1 and INS and chromosome Xq marker DXS52.
Academic Article A genetic linkage map of 17 markers on human chromosome 21.
Academic Article Peripherin gene is linked to keratin 18 gene on human chromosome 12.
Concept Genetic Linkage
Search Criteria
  • Genetic Linkage
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.