Chromosomes, Human, Pair 20
"Chromosomes, Human, Pair 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.
A specific pair of GROUP F CHROMOSOMES of the human chromosome classification.
Descriptor ID |
D002890
|
MeSH Number(s) |
A11.284.187.520.300.460.470 G05.360.162.520.300.460.470
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 20".
- Anatomy [A]
- Cells [A11]
- Cellular Structures [A11.284]
- Chromosomes [A11.284.187]
- Chromosomes, Mammalian [A11.284.187.520]
- Chromosomes, Human [A11.284.187.520.300]
- Chromosomes, Human, 19-20 [A11.284.187.520.300.460]
- Chromosomes, Human, Pair 20 [A11.284.187.520.300.460.470]
- Biological Sciences [G]
- Genetic Phenomena [G05]
- Genetic Structures [G05.360]
- Chromosomes [G05.360.162]
- Chromosomes, Mammalian [G05.360.162.520]
- Chromosomes, Human [G05.360.162.520.300]
- Chromosomes, Human, 19-20 [G05.360.162.520.300.460]
- Chromosomes, Human, Pair 20 [G05.360.162.520.300.460.470]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 20".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 20" by people in this website by year, and whether "Chromosomes, Human, Pair 20" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2003 | 1 | 0 | 1 |
2006 | 0 | 1 | 1 |
2008 | 1 | 0 | 1 |
2011 | 1 | 0 | 1 |
2012 | 1 | 0 | 1 |
2013 | 1 | 0 | 1 |
2016 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 20" by people in Profiles.
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Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes. BMC Med Genet. 2016 Mar 11; 17:20.
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Isolated hypermethylation of GRB10 (7p12.2) in a Silver-Russell syndrome patient carrying a 20p13 microdeletion. Clin Genet. 2014 Apr; 85(4):399-400.
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Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss. Br J Dermatol. 2012 Jun; 166(6):1314-8.
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Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome. Breast Cancer Res Treat. 2011 Dec; 130(3):905-16.
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Susceptibility variants for male-pattern baldness on chromosome 20p11. Nat Genet. 2008 Nov; 40(11):1279-81.
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Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation. Eur J Hum Genet. 2007 Jan; 15(1):35-44.
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Distal monosomy 18p/distal trisomy 20p--a recognizable facial phenotype? Am J Med Genet A. 2003 Jul 30; 120A(3):429-33.