Novel BCOR mutations in patients with oculofaciocardiodental (OFCD) syndrome

被引：26

作者：

Feberwee, H. E. ^{[1
]}

Feenstra, I. ^{[2
]}

Oberoi, S. ^{[3
]}

Sama, I. E. ^{[1
]}

Ockeloen, C. W. ^{[2
]}

Kuijpers, M. A. R. ^{[1
]}

Dooijes, D. ^{[4
]}

Kuijpers-Jagtman, A. M. ^{[1
]}

Kleefstra, T. ^{[2
]}

Carels, C. E. L. ^{[1
]}

机构：

[1] Radboud Univ Nijmegen, Med Ctr, Dept Orthodont & Craniofacial Biol, NL-6525 EX Nijmegen, Netherlands

[2] Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 EX Nijmegen, Netherlands

[3] Univ Calif San Francisco, Ctr Craniofacial Anomalies, San Francisco, CA 94143 USA

[4] Univ Med Ctr Utrecht, Dept Med Genet, Utrecht, Netherlands

来源：

CLINICAL GENETICS | 2014年 / 85卷 / 02期

关键词：

D O I：

10.1111/cge.12125

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：194 / 197

页数：4

共 8 条

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