Goldenhar Syndrome phenotypes and 22q11 deletion

被引：4

作者：

Balci, Sevim ^{[1
]}

Engiz, Ozlem ^{[1
]}

机构：

[1] Hacettepe Univ, Dept Clin Genet, Fac Med, TR-06100 Ankara, Turkey

来源：

关键词：

CHILD;

D O I：

10.1002/ajmg.a.33754

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：458 / 458

页数：1

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