"Chromosome Aberrations" 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.
Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS.
| Descriptor ID |
D002869
|
| MeSH Number(s) |
C23.550.210 G05.365.590.175
|
| Concept/Terms |
Chromosome Aberrations- Chromosome Aberrations
- Aberration, Chromosome
- Aberrations, Chromosome
- Chromosome Aberration
- Abnormalities, Chromosome
- Abnormality, Chromosome
- Chromosome Abnormality
- Cytogenetic Abnormalities
- Abnormalities, Cytogenetic
- Abnormality, Cytogenetic
- Cytogenetic Abnormality
- Chromosome Abnormalities
- Cytogenetic Aberrations
- Aberration, Cytogenetic
- Aberrations, Cytogenetic
- Cytogenetic Aberration
- Abnormalities, Chromosomal
- Abnormality, Chromosomal
- Chromosomal Abnormalities
- Chromosomal Abnormality
- Chromosomal Aberrations
- Aberration, Chromosomal
- Aberrations, Chromosomal
- Chromosomal Aberration
|
Below are MeSH descriptors whose meaning is more general than "Chromosome Aberrations".
Below are MeSH descriptors whose meaning is more specific than "Chromosome Aberrations".
This graph shows the total number of publications written about "Chromosome Aberrations" by people in this website by year, and whether "Chromosome Aberrations" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 0 | 1 | 1 |
| 2002 | 1 | 1 | 2 |
| 2007 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2014 | 0 | 1 | 1 |
| 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Chromosome Aberrations" by people in Profiles.
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Atypical and ultra-rare Usher syndrome: a review. Ophthalmic Genet. 2020 10; 41(5):401-412.
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Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk. Alzheimers Dement. 2016 Mar; 12(3):233-43.
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Multitarget stool DNA testing for colorectal-cancer screening. N Engl J Med. 2014 Apr 03; 370(14):1287-97.
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Performance on the Modified Card Sorting Test and its relation to psychopathology in adolescents and young adults with 22q11.2 deletion syndrome. J Intellect Disabil Res. 2009 Jul; 53(7):665-76.
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Correlating routine cytology, quantitative nuclear morphometry by digital image analysis, and genetic alterations by fluorescence in situ hybridization to assess the sensitivity of cytology for detecting pancreatobiliary tract malignancy. Am J Clin Pathol. 2007 Aug; 128(2):272-9.
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Clinical significance of alterations of chromosome 8 detected by fluorescence in situ hybridization analysis in pathologic organ-confined prostate cancer. Genes Chromosomes Cancer. 2002 Aug; 34(4):363-71.
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Loss of p53 and c-myc overrepresentation in stage T(2-3)N(1-3)M(0) prostate cancer are potential markers for cancer progression. Mod Pathol. 2002 Jan; 15(1):35-44.
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Holoprosencephaly: epidemiologic and clinical characteristics of a California population. Am J Med Genet. 1996 Aug 23; 64(3):465-72.