- chromosome breakage
- chromosome breakage.См. хромосомный разрыв.(Источник: «Англо-русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд-во ВНИРО, 1995 г.)
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chromosome breakage
Смотреть что такое "chromosome breakage" в других словарях:
chromosome breakage — chromosomos trūkis statusas T sritis augalininkystė apibrėžtis Abiejų vienos chromosomos chromatidžių nutrūkimas. atitikmenys: angl. chromosome break; chromosome breakage rus. хромосомный разрыв … Žemės ūkio augalų selekcijos ir sėklininkystės terminų žodynas
chromosome — chromosomal, adj. chromosomally, adv. /kroh meuh sohm /, n. Genetics. any of several threadlike bodies, consisting of chromatin, that carry the genes in a linear order: the human species has 23 pairs, designated 1 to 22 in order of decreasing… … Universalium
Chromosome 1, 1p36 deletion syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 34535 ICD10 = ICD9 = ICDO = OMIM = 607872 MedlinePlus = eMedicineSubj = eMedicineTopic = eMedicine mult = MeshID = Chromosome 1, 1p36 deletion syndrome is a medical condition caused by a rare … Wikipedia
chromosome break — chromosomos trūkis statusas T sritis augalininkystė apibrėžtis Abiejų vienos chromosomos chromatidžių nutrūkimas. atitikmenys: angl. chromosome break; chromosome breakage rus. хромосомный разрыв … Žemės ūkio augalų selekcijos ir sėklininkystės terminų žodynas
Chromosome instability syndrome — Chromosome instability syndromes are a group of inherited conditions associated with chromosomal instability and breakage. They often lead to an increased tendency to develop certain types of malignancies.[1] The following chromosome instability… … Wikipedia
Chromosome 22 (human) — Chromosome 22 is one of the 23 pairs of chromosomes in human cells. Humans normally have two copies of Chromosome 22 in each cell. Chromosome 22 is the second smallest human chromosome, spanning about 49 million DNA base pairs and representing… … Wikipedia
Chromosome abnormality — The three major single chromosome mutations; deletion (1), duplication (2) and inversion (3) … Wikipedia
Chromosome — A visible carrier of the genetic information. The 3 billion bp (base pairs) in the human genome are organized into 24 distinct, physically separate microscopic units called chromosomes. All genes are arranged linearly along the chromosomes. The… … Medical dictionary
Nijmegen breakage syndrome — A genetic disease named for the city of Nijmegen (in The Netherlands) with increased chromosome breakage, immunodeficiency and an increased risk of malignancy. Children with the syndrome appear abnormal with stunted growth before and after birth … Medical dictionary
Nijmegen breakage syndrome — Classification and external resources OMIM 251260 DiseasesDB 32395 eMedicine … Wikipedia
