- heterogeneity in the gene locus
- генетическая гетерогенность
English-Russian small dictionary of medicine. Г.Ю. Бельман, А.Е. Бойков.. 2015.
heterogeneity in the gene locus
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Allelic heterogeneity — The phenomenon in which different mutations at the same locus (or gene) cause the same disorder. For example,β thalessemia may be caused by several different mutations in the β globin gene … Wikipedia
Cream gene — Perlino redirects here. For the Polish village, see Perlino, Poland. The action of the cream gene on a chestnut base coat produces palomino … Wikipedia
RP2 (gene) — Retinitis pigmentosa 2 (X linked recessive), also known as RP2, is a human gene.cite web | title = Entrez Gene: RP2 retinitis pigmentosa 2 (X linked recessive)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… … Wikipedia
COL11A2 (gene) — Collagen, type XI, alpha 2, also known as COL11A2, is a human gene.cite web | title = Entrez Gene: COL11A2 collagen, type XI, alpha 2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=1302| accessdate = ] PBB … Wikipedia
AAAS (gene) — Achalasia, adrenocortical insufficiency, alacrimia (Allgrove, triple A), also known as AAAS, is a human gene responsible for Triple A syndrome (also known as Allgrove Syndrome).cite web | title = Entrez Gene: AAAS achalasia, adrenocortical… … Wikipedia
NHS (gene) — Nance Horan syndrome (congenital cataracts and dental anomalies) Identifiers Symbols NHS; CXN; DKFZp781F2016; DKFZp781L0254; FLJ22511; SCML1 External IDs … Wikipedia
STS (gene) — Steroid sulfatase (microsomal), arylsulfatase C, isozyme S, also known as STS, is a human gene.cite web | title = Entrez Gene: STS steroid sulfatase (microsomal), arylsulfatase C, isozyme S| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… … Wikipedia
evolution — evolutional, adj. evolutionally, adv. /ev euh looh sheuhn/ or, esp. Brit., /ee veuh /, n. 1. any process of formation or growth; development: the evolution of a language; the evolution of the airplane. 2. a product of such development; something… … Universalium
DISC1 — Disrupted in schizophrenia 1 Identifiers Symbols DISC1; C1orf136; FLJ13381; FLJ21640; FLJ25311; FLJ41105; KIAA0457; SCZD9 External IDs … Wikipedia
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
Dominant white — This dominant white Thoroughbred stallion (W2/+) has one form of dominant white. His skin, hooves, and coat lack pigment cells, giving him a pink skinned white coat. Dominant white is a group of genetically related coat color conditions in the… … Wikipedia
