Chromosomes, Human, 13-15
"Chromosomes, Human, 13-15" 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 medium-sized, acrocentric human chromosomes, called group D in the human chromosome classification. This group consists of chromosome pairs 13, 14, and 15.
|Chromosomes, Human, 13-15
- Chromosomes, Human, 13-15
- Group D Chromosomes
- Chromosome, Group D
- Chromosomes, Group D
- Group D Chromosome
- Chromosomes D
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, 13-15".
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, 13-15".
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Below are the most recent publications written about "Chromosomes, Human, 13-15" by people in Profiles.
Absence of SYCP3 mutations in women with recurrent miscarriage with at least one trisomic miscarriage. Reprod Biomed Online. 2012 Feb; 24(2):251-3.
Cigarette smoking, familial hematopoietic cancer, hair dye use, and risk of t(14;18)-defined subtypes of non-Hodgkin's lymphoma. Am J Epidemiol. 2007 Mar 15; 165(6):652-9.
Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13. Proc Natl Acad Sci U S A. 1986 Sep; 83(17):6573-7.
Molecular cloning of the breakpoint junction of a human chromosomal 8;14 translocation involving the T-cell receptor alpha-chain gene and sequences on the 3' side of MYC. Proc Natl Acad Sci U S A. 1986 Sep; 83(17):6636-40.
Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genes. Proc Natl Acad Sci U S A. 1986 Jul; 83(13):4864-8.
Gene encoding the alpha chain of the T-cell receptor is moved immediately downstream of c-myc in a chromosomal 8;14 translocation in a cell line from a human T-cell leukemia. Proc Natl Acad Sci U S A. 1986 May; 83(10):3439-43.
Constitutional t(15;17): clarification of the chromosomal breakpoints. Cancer Genet Cytogenet. 1986 Feb 01; 20(1-2):175-7.
Chromosome 13 homozygosity in osteosarcoma without retinoblastoma. Am J Hum Genet. 1986 Jan; 38(1):59-66.
A 14;19 translocation in B-cell chronic lymphocytic leukemia: a new recurring chromosome aberration. Int J Cancer. 1985 Sep 15; 36(3):287-90.
Translocation of the p53 gene in t(15;17) in acute promyelocytic leukaemia. Nature. 1985 Aug 29-Sep 4; 316(6031):826-8.