chromosomal breakage

chromosomal breakage
хромосомный разрыв

English-Russian small dictionary of medicine. . 2015.

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  • Chromosomal crossover — Thomas Hunt Morgan s illustration of crossing over (1916) A double cros …   Wikipedia

  • Chromosomal inversion — A clay model showing why heterozygous inversion loops are visible in polytene chromosome preparations …   Wikipedia

  • Chromosomal fragile site — Silencing of the FMR1 gene in Fragile X syndrome. FMR1 co localizes with a rare fragile site, visible here as a gap on the long arms of the X chromosome. A chromosomal fragile site is a specific heritable point on a chromosome that tends to form… …   Wikipedia

  • 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


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