terminal deletion

terminal deletion
loss of a segment from the end of a chromosome arm. See illustration at aberration.

Medical dictionary. 2011.

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  • terminal deletion — terminal deletion. См. терминальная делеция. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) …   Молекулярная биология и генетика. Толковый словарь.

  • Deletion (genetics) — Deletion on a chromosome In genetics, a deletion (also called gene deletion, deficiency, or deletion mutation) (sign: Δ) is a mutation (a genetic aberration) in which a part of a chromosome or a sequence of DNA is missing. Deletion is the loss of …   Wikipedia

  • Deletion — Loss of a segment of DNA from a chromosome (and hence from the genome). The first human chromosome deletion was detected in 1963 by Jerome Lejeune and his colleagues in Paris. They discovered loss of part of 5p, the short (p) arm of chromosome 5 …   Medical dictionary

  • 22q13 deletion syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = ICD10 = ICD9 = ICDO = OMIM = 606232 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = 22q13 Deletion Syndrome (spoken as twenty two q one three ), also known as Phelan McDermid Syndrome …   Wikipedia

  • 1p36 deletion syndrome — Classification and external resources A toddler showing facial symptoms of the syndrome. OMIM 607872 DiseasesDB …   Wikipedia

  • 9q34 deletion syndrome — Classification and external resources OMIM 610253 DiseasesDB 32302 9q34 deletion syndrome, also known as Kleefstra syndrome, is a …   Wikipedia

  • Ubiquitin carboxy-terminal hydrolase L1 — (UCH L1) (EC number|3.1.2.15) is a deubiqutinating enzyme. PBB Summary section title = summary text = UCHL1 is a member of a gene family whose products hydrolyze small C terminal adducts of ubiquitin to generate the ubiquitin monomer. Expression… …   Wikipedia

  • терминальная делеция — terminal deletion терминальная делеция. Делеция концевого участка хромосомы хромосомная аберрация, сопровождающаяся 1 хромосомным разрывом. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва:… …   Молекулярная биология и генетика. Толковый словарь.

  • List of diseases (C) — A list of diseases in the English wikipedia.C* C syndrome * C1 esterase deficiency (angioedema)CaCac Cal* Cacchi Ricci disease * CACH syndrome * Cafe au lait spots syndrome * Caffey disease * CAHMR syndrome * Calcinosis cutis (see also CREST… …   Wikipedia

  • Lujan-Fryns syndrome — Lujan–Fryns syndrome Classification and external resources Lujan–Fryns syndrome in a young adult male, with features that include a long, narrow face and recessed chin. ICD 10 F …   Wikipedia

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