 Chromosome Fragility
"Chromosome Fragility" 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.
Susceptibility of chromosomes to breakage leading to translocation; CHROMOSOME INVERSION; SEQUENCE DELETION; or other CHROMOSOME BREAKAGE related aberrations.
| Descriptor ID |
D002873
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| MeSH Number(s) |
C23.550.210.110.180 C23.550.362.180.180 G05.365.590.175.165.180 G05.370.180.180
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| Concept/Terms |
Chromosome Fragility- Chromosome Fragility
- Fragility, Chromosome
- Chromosomal Fragility
- Fragility, Chromosomal
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Below are MeSH descriptors whose meaning is more general than "Chromosome Fragility".
Below are MeSH descriptors whose meaning is more specific than "Chromosome Fragility".
This graph shows the total number of publications written about "Chromosome Fragility" by people in this website by year, and whether "Chromosome Fragility" 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 |
|---|
| 1987 | 1 | 0 | 1 | | 1988 | 0 | 1 | 1 | | 1998 | 0 | 1 | 1 | | 2014 | 1 | 0 | 1 |
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Below are the most recent publications written about "Chromosome Fragility" by people in Profiles.
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Grabowska-Joachimiak A, Kula A, Gernand-Kliefoth D, Joachimiak AJ. Karyotype structure and chromosome fragility in the grass Phleum echinatum Host. Protoplasma. 2015 Jan; 252(1):301-6.
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Sato Y, Kobayashi H, Suto Y, Olney HJ, Davis EM, Super HG, Espinosa R, Le Beau MM, Rowley JD. Chromosomal instability in chromosome band 12p13: multiple breaks leading to complex rearrangements including cytogenetically undetectable sub-clones. Leukemia. 2001 Aug; 15(8):1193-202.
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Gleeson JG, Allen KM, Fox JW, Lamperti ED, Berkovic S, Scheffer I, Cooper EC, Dobyns WB, Minnerath SR, Ross ME, Walsh CA. Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein. Cell. 1998 Jan 09; 92(1):63-72.
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DeLisi LE, Reiss AL, White BJ, Gershon ES. Cytogenetic studies of males with schizophrenia. Screening for the fragile X chromosome and other chromosomal abnormalities. Schizophr Res. 1988 Jul-Aug; 1(4):277-81.
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Amarose AP, Huttenlocher PR, Sprudzs RM, Laitsch TJ, Pettenati MJ. A heritable fragile 12q24.13 segregating in a family with the fragile X chromosome. Hum Genet. 1987 Jan; 75(1):4-6.
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