The Opitz syndrome gene product, MID1, interacts with the gene product of an X-chromosomal gene mapping to the linkage interval of FG syndrome.

被引：0
|
作者：
Schweiger, S
Trockenbacher, A
Suckow, V
Krau, S
Ropers, HH
Schneider, R
机构：
[1] Max Planck Inst Mol Genet, Berlin, Germany
[2] Univ Innsbruck, Inst Biochem, A-6020 Innsbruck, Austria
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：
919
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页码：174 / 174
页数：1
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