Definition(s)
- An exchange of homologous segments of genetic material between the sister chromatids of a chromosome, either between the sister chromatids of a meiotic tetrad or between the sister chromatids of a duplicated somatic chromosome. Its frequency is increased as a result of inordinate chromosomal fragility due to genetic or environmental factors such as ultraviolet or ionizing radiation and other mutagenic agents, and is particularly high in Bloom Syndrome.
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Definition from: NCI Thesaurus via Unified Medical Language System
at the National Library of Medicine
See also Understanding Medical Terminology.