Chromosomes, Human, 6-12 and X
"Chromosomes, Human, 6-12 and X" 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, submetacentric human chromosomes, called group C in the human chromosome classification. This group consists of chromosome pairs 6, 7, 8, 9, 10, 11, and 12 and the X chromosome.
MeSH Number(s)
A11.284.187.520.300.325
G05.360.162.520.300.325
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, 6-12 and X".
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, 6-12 and X".
- Chromosomes, Human, 6-12 and X
- Chromosomes, Human, Pair 10
- Chromosomes, Human, Pair 11
- Chromosomes, Human, Pair 12
- Chromosomes, Human, Pair 6
- Chromosomes, Human, Pair 7
- Chromosomes, Human, Pair 8
- Chromosomes, Human, Pair 9
- Chromosomes, Human, X
This graph shows the total number of publications written about "Chromosomes, Human, 6-12 and X" by people in Harvard Catalyst Profiles by year, and whether "Chromosomes, Human, 6-12 and X" 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 |
|---|
| 2000 | 0 | 1 | 1 |
| 2008 | 1 | 0 | 1 |
Below are the most recent publications written about "Chromosomes, Human, 6-12 and X" by people in Profiles.
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Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study. Lancet. 2008 Dec 06; 372(9654):1953-61.
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Dysregulation of HMGIC in a uterine lipoleiomyoma with a complex rearrangement including chromosomes 7, 12, and 14. Genes Chromosomes Cancer. 2000 Feb; 27(2):209-15.
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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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PvuII polymorphic site upstream to the human ApoCIII gene. Nucleic Acids Res. 1986 Jul 11; 14(13):5571.
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Deletion of the steroid 21-hydroxylase and complement C4 genes in congenital adrenal hyperplasia. J Med Genet. 1986 Jun; 23(3):204-9.
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The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus. Nature. 1986 Jun 26-Jul 2; 321(6073):882-7.
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Recurrent chromosome translocations in liposarcoma. Cancer Genet Cytogenet. 1986 May; 22(1):93-4.
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Human inhibitor of the first component of complement, C1: characterization of cDNA clones and localization of the gene to chromosome 11. Proc Natl Acad Sci U S A. 1986 May; 83(10):3161-5.
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Congenital heart disease in supernumerary der(22),t(11;22) syndrome. Clin Genet. 1986 Apr; 29(4):269-75.
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The nucleotide and derived amino acid sequence of human apolipoprotein A-IV mRNA and the close linkage of its gene to the genes of apolipoproteins A-I and C-III. J Biol Chem. 1986 Feb 15; 261(5):1998-2002.