"Chromosome Breakage" 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.
A type of chromosomal aberration involving DNA BREAKS. Chromosome breakage can result in CHROMOSOMAL TRANSLOCATION; CHROMOSOME INVERSION; or SEQUENCE DELETION.
| Descriptor ID |
D019457
|
| MeSH Number(s) |
C23.550.210.170 G05.200.210.170 G05.365.590.175.175
|
| Concept/Terms |
Chromosome Breakage- Chromosome Breakage
- Breakage, Chromosome
- Breakages, Chromosome
- Chromosome Breakages
- Chromosomal Breakage
- Breakage, Chromosomal
- Breakages, Chromosomal
- Chromosomal Breakages
Chromosome Breaks- Chromosome Breaks
- Break, Chromosome
- Breaks, Chromosome
- Chromosome Break
- Chromosomal Breaks
- Break, Chromosomal
- Breaks, Chromosomal
- Chromosomal Break
|
Below are MeSH descriptors whose meaning is more general than "Chromosome Breakage".
Below are MeSH descriptors whose meaning is more specific than "Chromosome Breakage".
This graph shows the total number of publications written about "Chromosome Breakage" by people in this website by year, and whether "Chromosome Breakage" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2000 | 1 | 0 | 1 |
| 2003 | 1 | 0 | 1 |
| 2006 | 0 | 1 | 1 |
| 2007 | 1 | 0 | 1 |
| 2010 | 0 | 1 | 1 |
| 2013 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosome Breakage" by people in Profiles.
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Cytogenetic aspects of childhood leukemias. Klin Padiatr. 2013 May; 225 Suppl 1:S30-3.
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Genotype-phenotype correlation in eight new patients with a deletion encompassing 2q31.1. Am J Med Genet A. 2010 May; 152A(5):1213-24.
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Identification of two distinct MYC breakpoint clusters and their association with various IGH breakpoint regions in the t(8;14) translocations in sporadic Burkitt-lymphoma. Leukemia. 2007 Aug; 21(8):1739-51.
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Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation. Eur J Hum Genet. 2007 Jan; 15(1):35-44.
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Analysis of t(9;11) chromosomal breakpoint sequences in childhood acute leukemia: almost identical MLL breakpoints in therapy-related AML after treatment without etoposides. Genes Chromosomes Cancer. 2003 Apr; 36(4):393-401.
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A deletion distinct from the classical homologous recombination of juvenile nephronophthisis type 1 (NPH1) allows exact molecular definition of deletion breakpoints. Hum Mutat. 2000 Sep; 16(3):211-23.
MeSH information
