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1 chromosomal breakage
1. Разрыв, одновременно происходящий в одних и тех же местах у двух хроматид одной хромосомы.2. Одна из форм хромосомных аберраций, произошедшая до их репликации.Англо-русский толковый словарь генетических терминов > chromosomal breakage
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2 chromosomal breakage
English-Russian small dictionary of medicine > chromosomal breakage
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3 chromosomal breakage syndromes
Медицина: синдромы "поломок хромосом", синдромы нестабильности генома, синдромы хромосомной нестабильности (генетические заболевания, проявляющиеся неустойчивостью хромосом in vitro и склонностью к определенным новообразованиям), синдромы хромосомных разрывовУниверсальный англо-русский словарь > chromosomal breakage syndromes
См. также в других словарях:
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chromosomal mutation — a mutation affecting large regions of a chromosome and caused by breakage, e.g., by deletion, inversion, or translocation. See also genomic m. and point m … Medical dictionary
Nijmegen-Breakage-Syndrom — Das Nijmegen Breakage Syndrom (Abkürzung: NBS; englisch: Nijmegen breakage syndrome) ist eine syndromale, seltene, angeborene Krankheit des Menschen mit einer Störung des Reparaturmechanismus der Erbsubstanz (DNA) in allen Zellen und Organen mit… … Deutsch Wikipedia
Nijmegen breakage syndrome — Classification and external resources OMIM 251260 DiseasesDB 32395 eMedicine … Wikipedia
Nijmegen breakage syndrome — Syndrome de Nimègue Syndrome de Nimègue Autre nom Microcéphalie immunodéficience – lymphoréticulome Syndrome de Seemanova, type 2 Référence MIM … Wikipédia en Français
Nijmegen breakage syndrome — Autosomal recessive chromosomal instability syndrome characterized by microencephaly, growth retardation, immunodeficiency, and predisposition to tumours. Cells from patients are hypersensitive to ionizing radiation in the same way as cells from… … Dictionary of molecular biology
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
genetics — /jeuh net iks/, n. (used with a sing. v.) 1. Biol. the science of heredity, dealing with resemblances and differences of related organisms resulting from the interaction of their genes and the environment. 2. the genetic properties and phenomena… … Universalium
FANCD2 — Fanconi anemia, complementation group D2, also known as FANCD2, is a human gene.cite web | title = Entrez Gene: FANCD2 Fanconi anemia, complementation group D2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… … Wikipedia
