 Ring Chromosomes
"Ring Chromosomes" 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.
Aberrant chromosomes with no ends, i.e., circular.
| Descriptor ID |
D012303
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| MeSH Number(s) |
A11.284.187.788 C23.550.210.760 G05.360.162.788 G05.365.590.175.760
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| Concept/Terms |
Ring Chromosomes- Ring Chromosomes
- Chromosomes, Ring
- Chromosome, Ring
- Ring Chromosome
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Below are MeSH descriptors whose meaning is more general than "Ring Chromosomes".
Below are MeSH descriptors whose meaning is more specific than "Ring Chromosomes".
This graph shows the total number of publications written about "Ring Chromosomes" by people in this website by year, and whether "Ring Chromosomes" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2016 | 0 | 1 | 1 |
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Below are the most recent publications written about "Ring Chromosomes" by people in Profiles.
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Byers HM, Adam MP, LaCroix A, Leary SE, Cole B, Dobyns WB, Mefford HC. Description of a new oncogenic mechanism for atypical teratoid rhabdoid tumors in patients with ring chromosome 22. Am J Med Genet A. 2017 Jan; 173(1):245-249.
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Rudd MK, Mays RW, Schwartz S, Willard HF. Human artificial chromosomes with alpha satellite-based de novo centromeres show increased frequency of nondisjunction and anaphase lag. Mol Cell Biol. 2003 Nov; 23(21):7689-97.
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Chawla J, Sucholeiki R, Jones C, Silver K. Intractable epilepsy with ring chromosome 20 syndrome treated with vagal nerve stimulation: case report and review of the literature. J Child Neurol. 2002 Oct; 17(10):778-80.
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Wolff DJ, Brown CJ, Schwartz S, Duncan AM, Surti U, Willard HF. Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations. Am J Hum Genet. 1994 Jul; 55(1):87-95.
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Duncan AM, Macdonald A, Brown CJ, Wolff D, Willard HF, Sutton B. Characterization of a small supernumerary ring X chromosome by fluorescence in situ hybridization. Am J Med Genet. 1993 Dec 01; 47(8):1153-6.
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Haaf T, Sumner AT, Köhler J, Willard HF, Schmid M, Summer AT. A microchromosome derived from chromosome 11 in a patient with the CREST syndrome of scleroderma. Cytogenet Cell Genet. 1992; 60(1):12-7.
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Koch J, Kølvraa S, Hobolt N, Petersen GB, Willard HF, Waye JS, Gregersen N, Bolund L. A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization. Clin Genet. 1990 Mar; 37(3):216-20.
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