FOXL2 mutations in Tunisian patients with blepharophimosis-ptosis-epicanthus inversus syndrome

被引：0
作者：
Kraoua, L. [2 ]
Chaabouni, M. [1 ]
Trabelsi, M. [1 ]
Chelly, I. [1 ]
Maazoul, F. [1 ]
Ben Abdallah, N. [1 ]
Boukthir, S. [3 ]
Barsaoui, S. [3 ]
Chaabouni, H. [1 ,2 ]
M'rad, R. [1 ,2 ]
机构：
[1] Hop Charles Nicolle, Dept Congenital & Hereditary Dis, Tunis 1007, Tunisia
[2] Fac Med Tunis, Dept Human Genet, Tunis, Tunisia
[3] Natl Inst Child Hlth, Tunis, Tunisia
来源：
CLINICAL GENETICS | 2010年 / 77卷 / 06期
关键词：
GENOTYPE-PHENOTYPE CORRELATION; PREMATURE OVARIAN FAILURE; CHINESE PATIENTS; BPES; GENE;
D O I：
10.1111/j.1399-0004.2010.01389.x
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：601 / 603
页数：3
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