一个以色列家庭中的镰状细胞性地中海贫血
Sickle cell thalassemia in an Israeli family.
作者信息
Dvilansky A, Zaizov R, Moses S
出版信息
Isr J Med Sci. 1976 Jun;12(6):543-7.
PMID:955870
Abstract
Sickle cell thalassemia in an Israeli family of Indian extraction is described. The family demonstrates the segregation of the betaS- and beta-thal genes and the interaction phenomenon known to exist in this condition is demonstrated clearly in the propositus.
摘要
本文描述了一个来自印度裔以色列家庭的镰状细胞地中海贫血病例。该家庭呈现出βS基因和β地中海贫血基因的分离现象，并且在先证者中清楚地展示了已知存在于这种病症中的相互作用现象。
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