Chromosomes, Human, 21-22 and Y
"Chromosomes, Human, 21-22 and Y" 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, acrocentric human chromosomes, called group G in the human chromosome classification. This group consists of chromosome pairs 21 and 22 and the Y chromosome.
MeSH Number(s)
A11.284.187.520.300.505
G05.360.162.520.300.505
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, 21-22 and Y".
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, 21-22 and Y".
This graph shows the total number of publications written about "Chromosomes, Human, 21-22 and Y" by people in Harvard Catalyst Profiles by year, and whether "Chromosomes, Human, 21-22 and Y" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2011 | 0 | 1 | 1 |
Below are the most recent publications written about "Chromosomes, Human, 21-22 and Y" by people in Profiles.
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Development of patient-specific neurons in schizophrenia using induced pluripotent stem cells. J Neurogenet. 2011 Oct; 25(3):88-103.
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[22q11.2 deficiency syndrome diagnosed with congestive heart failure]. Nihon Naika Gakkai Zasshi. 2008 Nov 10; 97(11):2785-7.
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Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching. J Am Coll Cardiol. 2001 Jun 15; 37(8):2114-9.
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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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Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma. Nature. 1986 Aug 14-20; 322(6080):644-7.
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The chronic myelogenous leukemia-specific P210 protein is the product of the bcr/abl hybrid gene. Science. 1986 Jul 11; 233(4760):212-4.
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Regional localization of DNA sequences on chromosome 21 using somatic cell hybrids. Am J Hum Genet. 1986 Jun; 38(6):793-804.
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DNA deletion in boy with Becker muscular dystrophy. Lancet. 1986 Apr 19; 1(8486):918.
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Translocation (13;22) in a hemangiopericytoma. Cancer Genet Cytogenet. 1986 Apr 15; 21(4):309-18.
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Congenital heart disease in supernumerary der(22),t(11;22) syndrome. Clin Genet. 1986 Apr; 29(4):269-75.