A SALL1 mutation causes a branchio-oto-renal syndrome-like phenotype

被引：49

作者：

Engels, S

Kohlhase, J

McGaughran, J

机构：

[1] Univ Gottingen, Inst Human Genet, D-37073 Gottingen, Germany

[2] Univ Auckland, Dept Med Genet, Auckland 1, New Zealand

来源：

JOURNAL OF MEDICAL GENETICS | 2000年 / 37卷 / 06期

关键词：

D O I：

10.1136/jmg.37.6.458

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：458 / 460

页数：3

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