uniparental disomy

uniparental disomy
uniparental disomy.
(Источник: «Англо-русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд-во ВНИРО, 1995 г.)


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  • Uniparental disomy — Infobox Disease Name = Uniparental disomy Caption = DiseasesDB = ICD10 = ICD10|Q|99|8|q|90 ICD9 = ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Uniparental disomy (UPD) occurs when a person receives two copies of a… …   Wikipedia

  • uniparental disomy — the abnormal state in which both copies of a homologous pair of chromosomes are from the same parent, with none from the other parent …   Medical dictionary

  • uniparental — uni·pa·ren·tal .yü ni pə rent əl adj having, involving, or derived from a single parent specif involving or being inheritance in which an offspring s complete genotype or all copies of one or more genes, chromosome parts, or whole chromosomes are …   Medical dictionary

  • однородительская дисомия — uniparental disomy однородительская дисомия. Происхождение пары гомологичных хромосом диплоидного организма из генома одного из родителей при половом размножении например, при слиянии дисомичной яйцеклетки и нуллисомичного спермия, дисомичной… …   Молекулярная биология и генетика. Толковый словарь.

  • Confined placental mosaicism — (CPM) represents a discrepancy between the chromosomal makeup of the cells in the placenta and the cells in the baby. CPM was first described by Kalousek and Dill in 1983.[1] CPM is diagnosed when some trisomic cells are detected on chorionic… …   Wikipedia

  • List of diseases (U) — A list of diseases in the English wikipedia.DiseasesTOC Ud Up* UDP galactose 4 epimerase deficiency * Uhl anomaly * Ulbright Hodes syndrome * Ulcerative colitis * Ulerythema ophryogenesis * Ulna and fibula absence with severe limb deficit * Ulna… …   Wikipedia

  • 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

  • Aneuploidy — Classification and external resources ICD 10 Q90 Q98 ICD 9 …   Wikipedia

  • genetic disease, human — Introduction       any of the diseases and disorders that are caused by mutations in one or more genes (gene).       With the increasing ability to control infectious and nutritional diseases in developed countries, there has come the realization …   Universalium

  • Prader–Willi syndrome — Prader Willi syndrome Classification and external resources ICD 10 Q87.1 ICD 9 759.81 …   Wikipedia

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