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 | 1 | 0 | 1 |
| 1999 | 0 | 1 | 1 |
| 2001 | 1 | 0 | 1 |
| 2009 | 0 | 1 | 1 |
| 2024 | 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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Klamut N, Bothwell S, Carl AE, Bamba V, Law JR, Brickman WJ, Klein KO, Kanakatti Shankar R, Pinnaro CT, Fechner PY, Prakash SK, Gutmark-Little I, Howell S, Tartaglia N, Good M, Ranallo KC, Davis SM. Prevalence, diagnostic features, and medical outcomes of females with Turner syndrome with a trisomy X cell line (45,X/47,XXX): Results from the InsighTS Registry. Am J Med Genet A. 2024 Dec; 194(12):e63819.
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Parva M, Donnenfeld AE, Gerson A. Trizygotic dichorionic triplets with 46,XX/46,XY chimerism in both fetuses of the monochorionic pair. Prenat Diagn. 2009 Nov; 29(11):1091-3.
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Zinn AR. The X chromosome and the ovary. J Soc Gynecol Investig. 2001 Jan-Feb; 8(1 Suppl Proceedings):S34-6.
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Melhem ER, Barker PB, Raymond GV, Moser HW. X-linked adrenoleukodystrophy in children: review of genetic, clinical, and MR imaging characteristics. AJR Am J Roentgenol. 1999 Dec; 173(6):1575-81.
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Ross JL, Kushner H, Zinn AR. Discriminant analysis of the Ullrich-Turner syndrome neurocognitive profile. Am J Med Genet. 1997 Oct 31; 72(3):275-80.
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Shivashankar L, Whitney E, Colmorgen G, Young T, Munshi G, Wilmoth D, Byrne K, Reeves G, Borgaonkar DS, Picciano SR, et al. Prenatal diagnosis of tetrasomy 47,XY,+i(12p) confirmed by in situ hybridization. Prenat Diagn. 1988 Feb; 8(2):85-91.
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Hernandez P, Hilty GR, Borgaonkar DS. A 47,XXX female with unusual phenotype. Del Med J. 1983 Nov; 55(11):661-3.
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Seegmiller JE, Siniscalco M, Klinger HP, Eagle H, Koprowski H, Fujimoto WY. Intergenomic complementation of two X-linked genes by hydridization of mutant human fibroblasts. Trans Assoc Am Physicians. 1969; 82:239-47.