Sex Chromosome Aberrations
"Sex 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 the SEX CHROMOSOMES. Some sex chromosome aberrations are associated with SEX CHROMOSOME DISORDERS and SEX CHROMOSOME DISORDERS OF SEX DEVELOPMENT.
| Descriptor ID |
D012729
|
| MeSH Number(s) |
C23.550.210.815 G05.365.590.175.815
|
| Concept/Terms |
Sex Chromosome Aberrations- Sex Chromosome Aberrations
- Aberration, Sex Chromosome
- Aberrations, Sex Chromosome
- Chromosome Aberration, Sex
- Chromosome Aberrations, Sex
- Sex Chromosome Aberration
- Sex Chromosome Abnormalities
- Abnormality, Sex Chromosome
- Chromosome Abnormality, Sex
- Sex Chromosome Abnormality
- Abnormalities, Sex Chromosome
- Chromosome Abnormalities, Sex
|
Below are MeSH descriptors whose meaning is more general than "Sex Chromosome Aberrations".
Below are MeSH descriptors whose meaning is more specific than "Sex Chromosome Aberrations".
This graph shows the total number of publications written about "Sex Chromosome Aberrations" by people in this website by year, and whether "Sex Chromosome Aberrations" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 2 | 1 | 3 |
| 1998 | 1 | 0 | 1 |
| 2001 | 1 | 0 | 1 |
| 2002 | 0 | 1 | 1 |
| 2010 | 1 | 0 | 1 |
| 2016 | 0 | 1 | 1 |
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Below are the most recent publications written about "Sex Chromosome Aberrations" by people in Profiles.
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X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome. Arthritis Rheumatol. 2016 05; 68(5):1290-1300.
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Maternal source of false-positive fetal sex chromosome aneuploidy in noninvasive prenatal testing. Obstet Gynecol. 2015 Feb; 125(2):390-392.
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The sex-specific region of sex chromosomes in animals and plants. Chromosome Res. 2012 Jan; 20(1):57-69.
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Evidence of a mechanism for isodicentric chromosome Y formation in a 45,X/46,X,idic(Y)(p11.31)/46,X,del(Y)(p11.31) mosaic karyotype. Eur J Med Genet. 2011 Mar-Apr; 54(2):161-4.
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A case of negative-pressure pulmonary edema after electroconvulsive therapy. J ECT. 2007 Dec; 23(4):281-3.
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Chromatin of the Barr body: histone and non-histone proteins associated with or excluded from the inactive X chromosome. Hum Mol Genet. 2003 Sep 01; 12(17):2167-78.
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Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies. Am J Hum Genet. 2003 Feb; 72(2):399-407.
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Biological functions of the ISWI chromatin remodeling complex NURF. Genes Dev. 2002 Dec 15; 16(24):3186-98.
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Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females. Hum Mol Genet. 2001 Aug 15; 10(17):1775-83.
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Histone variant macroH2A contains two distinct macrochromatin domains capable of directing macroH2A to the inactive X chromosome. Nucleic Acids Res. 2001 Jul 01; 29(13):2699-705.