[一名突尼斯儿童的双重杂合子 Hb O Arab/β地中海贫血]
[Double heterozygous Hb O Arab/beta-thalassemia in a Tunisian child].
作者信息
Haji F, Chadli A, Fattoum S, Souilem J, Hassine L
出版信息
Arch Inst Pasteur Tunis. 1985 Dec;62(4):341-53.
PMID:2423045
Abstract
A study realized in a Tunisian family of 22 persons has revealed a double heterozygoty Hb O Arab/beta(0) thalassemia in a child of 16 years old. The father of this child presents a beta thalassemia and his mother is haemoglobine O Arab homozygote.
摘要
在一个22人的突尼斯家庭中进行的一项研究发现，一名16岁儿童存在Hb O阿拉伯型/β(0)地中海贫血双重杂合子。该儿童的父亲患有β地中海贫血，其母亲是Hb O阿拉伯型纯合子。
Zotero 插件