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.
| Descriptor ID |
D002902
|
| 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 this website by year, and whether "Chromosomes, Human, 16-18" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2007 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, 16-18" by people in Profiles.
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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.
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Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps. Proc Natl Acad Sci U S A. 1986 Aug; 83(15):5611-5.
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Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome. Am J Med Genet. 1986 Jul; 24(3):421-32.
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Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17. Am J Med Genet. 1986 Apr; 23(4):853-9.
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Constitutional t(15;17): clarification of the chromosomal breakpoints. Cancer Genet Cytogenet. 1986 Feb 01; 20(1-2):175-7.
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Translocation of the p53 gene in t(15;17) in acute promyelocytic leukaemia. Nature. 1985 Aug 29-Sep 4; 316(6031):826-8.
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Localization of the oncogene c-erbA1 immediately proximal to the acute promyelocytic leukaemia breakpoint on chromosome 17. Ann Hum Genet. 1985 07; 49(3):167-71.
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Metallothionein gene cluster is split by chromosome 16 rearrangements in myelomonocytic leukaemia. Nature. 1985 Feb 21-27; 313(6004):709-11.
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Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly. Am J Med Genet. 1984 Jul; 18(3):509-26.
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A morphologic and cytochemical study of acute myelomonocytic leukemia with abnormal marrow eosinophils associated with inv(16)(p13q22). Am J Clin Pathol. 1984 Jun; 81(6):733-41.