A novel TBX3 frameshift mutation in a patient with Ulnar-Mammary syndrome.

被引：0
|
作者：
Jobard, A [1 ]
La Merrer, M [1 ]
Audollent, S [1 ]
Augé, J [1 ]
Martinovic, J [1 ]
Munnich, A [1 ]
Vekemans, M [1 ]
Attié-Bitach, T [1 ]
机构：
[1] Hop Necker Enfants Malad, INSERM, Dept Genet, U393, Paris, France
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2000年 / 67卷 / 04期
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D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
2132
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页码：381 / 381
页数：1
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