FRAGILE-X (BELL,MARTIN) SYNDROME IN AN IRANIAN FAMILY WITH 8 AFFECTED MEMBERS

被引：0
|
作者：
KARIMINEJAD, MH
RAHIMI, M
SHIRNESHAN, K
VAEZI, SA
KARIMINEJAD, R
机构：
[1] IRAN UNIV MED SCI,TEHRAN,IRAN
[2] KARIMI NEJAD PATHOL & GENET CTR,TEHRAN,IRAN
[3] TEHRAN PSYCHIAT INST,TEHRAN,IRAN
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1991年 / 49卷 / 04期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：267 / 267
页数：1
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