Congenital hypertelorism and osteopenia: A novel autosomal recessive disease

被引：0

作者：

Bonnard, Carine ^{[1
]}

Merriman, Barry ^{[2
]}

Lee, Hane ^{[2
]}

Kayserili, Hulya ^{[3
]}

Akarsu, Nurten ^{[4
]}

Strobl, Anna ^{[1
]}

Shboul, Mohammad ^{[1
]}

Hamamy, Hanan ^{[5
]}

Reversade, Bruno ^{[1
]}

机构：

[1] ASTAR, Inst Med Biol, Singapore, Singapore

[2] Univ Calif Los Angeles, Dept Human Genet, Los Angeles, CA USA

[3] Istanbul Fac Med, Dept Med Genet, Istanbul, Turkey

[4] Hacettepe Univ, Fac Med, Dept Med Genet, Sihhiye, Turkey

[5] Natl Ctr Diabet Endocrinol & Genet, Amman, Jordan

来源：

DIFFERENTIATION | 2010年 / 80卷

关键词：

D O I：

10.1016/j.diff.2010.09.112

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

引用

页码：S52 / S52

页数：1

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