Chromosomes, Human, 16-18
"Chromosomes, Human, 16-18" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The short, submetacentric human chromosomes, called group E in the human chromosome classification. This group consists of chromosome pairs 16, 17, and 18.
MeSH Number(s)
A11.284.187.520.300.415
G05.360.162.520.300.415
Concept/Terms
Chromosomes, Human, 16-18- Chromosomes, Human, 16-18
- Group E Chromosomes
- Chromosome, Group E
- Chromosomes, Group E
- E Chromosomes, Group
- Group E Chromosome
- Chromosomes E
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, 16-18".
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, 16-18".
This graph shows the total number of publications written about "Chromosomes, Human, 16-18" by people in Harvard Catalyst Profiles by year, and whether "Chromosomes, Human, 16-18" was a major or minor topic of these publication.
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Below are the most recent publications written about "Chromosomes, Human, 16-18" by people in Profiles.
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LFA-1 immunodeficiency disease. Definition of the genetic defect and chromosomal mapping of alpha and beta subunits of the lymphocyte function-associated antigen 1 (LFA-1) by complementation in hybrid cells. J Exp Med. 1986 Sep 01; 164(3):855-67.
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Translocation X;18 in synovial sarcoma. Cancer Genet Cytogenet. 1986 Sep; 23(1):93.
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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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A new RFLP for D18S3(B74) an anonymous genomic clone localized to 18p113. Nucleic Acids Res. 1986 Aug 26; 14(16):6782.
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t(Y;18) in acute myeloblastic leukemia FAB type M2. Cancer Genet Cytogenet. 1986 Aug; 22(4):367-8.
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Antenatal sonographic findings in trisomy 18. J Ultrasound Med. 1986 Jul; 5(7):361-4.
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Abnormal facial features and extremities in human trisomy syndromes: prenatal US appearance. Radiology. 1986 Apr; 159(1):243-6.
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Tyrosine kinase receptor with extensive homology to EGF receptor shares chromosomal location with neu oncogene. Science. 1985 Dec 06; 230(4730):1132-9.
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Transformation associated p53 protein is encoded by a gene on human chromosome 17. Somat Cell Mol Genet. 1985 Sep; 11(5):505-10.
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DNA polymorphism and molecular pathology of the human globin gene clusters. Hum Genet. 1985; 69(1):1-14.