+p9综合征的遗传学
Genetics of the +p9 syndrome.
作者信息
Lurie I W, Lazjuk G I, Gurevich D B, Usoev S S
出版信息
Hum Genet. 1976 Apr 15;32(1):23-33. doi: 10.1007/BF00569973.
PMID:770307
Abstract
An analysis of data about the +p9 syndrome revealed that this clinical entity may occur in some different genetic forms. The recurrence risk in cases with familial translocations is due to the type of meiotic segregation, 2:2 or 3:1. It was shown a nonrandomness of involvement of chromosomes 15 and 22 in translocations with chromosome number 9.
摘要
对+p9综合征数据的分析显示，这种临床实体可能以几种不同的遗传形式出现。家族性易位病例的复发风险取决于减数分裂分离的类型，即2:2或3:1。研究表明，15号和22号染色体在与9号染色体的易位中存在非随机性参与。
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