Mutations in the CHX10 gene in non-syndromic microphthalmia/anophthalmia patients from Qatar

被引：24

作者：

Faiyaz-Ul-Haque, M.

Zaidi, S. H. E.

Al-Mureikhi, M. S.

Peltekova, I.

Tsui, L-C

Teebi, A. S.

机构：

[1] King Faisal Specialist Hosp & Res Ctr, Dept Pathol & Lab Med, Genet Mol Lab, Riyadh 11211, Saudi Arabia

[2] Hosp Sick Children, Dept Genet, Program Genet & Genom Biol, Toronto, ON M5G 1X8, Canada

[3] Weill Cornell Med Coll Qatar, Dept Med Genet, Doha, Qatar

[4] Univ Toronto, Dept Med, Toronto, ON, Canada

[5] Hamad Med Corp, Dept Pediat, Doha, Qatar

[6] Univ Hong Kong, Hong Kong, Hong Kong, Peoples R China

[7] Weill Cornell Med Coll Qatar, Dept Pediat, Education City, Doha, Qatar

[8] Weill Cornell Med Coll Qatar, Dept Med Genet, Education City, Doha, Qatar

来源：

CLINICAL GENETICS | 2007年 / 72卷 / 02期

关键词：

D O I：

10.1111/j.1399-0004.2007.00846.x

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：164 / 166

页数：3

共 11 条

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