Chromosomes, Human, 19-20
"Chromosomes, Human, 19-20" 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, metacentric human chromosomes, called group F in the human chromosome classification. This group consists of chromosome pairs 19 and 20.
| Descriptor ID |
D002903
|
| MeSH Number(s) |
A11.284.187.520.300.460 G05.360.162.520.300.460
|
| Concept/Terms |
Chromosomes, Human, 19-20- Chromosomes, Human, 19-20
- Group F Chromosomes
- Chromosome, Group F
- Chromosomes, Group F
- Group F Chromosome
- Chromosomes F
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, 19-20".
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, 19-20".
This graph shows the total number of publications written about "Chromosomes, Human, 19-20" by people in this website by year, and whether "Chromosomes, Human, 19-20" was a major or minor topic of these publications.
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Below are the most recent publications written about "Chromosomes, Human, 19-20" by people in Profiles.
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Prognostic implications of morphology and karyotype in primary myelodysplastic syndromes. Blood. 1986 Jun; 67(6):1765-72.
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c-src is consistently conserved in the chromosomal deletion (20q) observed in myeloid disorders. Proc Natl Acad Sci U S A. 1985 Oct; 82(19):6692-6.
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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.
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Regional localization of the phosphoglycerate kinase gene and pseudogene on the human X chromosome and assignment of a related DNA sequence to chromosome 19. Hum Genet. 1985; 71(2):138-43.
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Evidence for two distinct c-src loci on human chromosomes 1 and 20. Nature. 1984 Nov 1-7; 312(5989):70-1.
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Multiple cytogenetically abnormal clones in two polycythemia vera patients. Hum Genet. 1981; 57(2):165-8.
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Karyotypic patterns and their clinical significance in polycythemia vera. Am J Hematol. 1981; 11(1):29-45.
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Chromosomal DNA cytophotometry in 20q- nonspecific myeloid disorders. Cancer Res. 1979 Aug; 39(8):2984-7.
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Chromosome abnormalities in the acute phase of CML. Virchows Arch B Cell Pathol. 1978 Nov 17; 29(1-2):57-63.
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Deletion of the long arm of chromosome 20 [del(20)(q11)] in myeloid disorders. Blood. 1978 Nov; 52(5):868-77.