Russell-Silver syndrome as a phenotype resulting from defects in the IGF1R axis: the ligand IGF2, its receptor IGF1R, or the signaling modulator GRB10.

被引：0
|
作者：
Kosaki, K
Kikuchi, T
Yoshihashi, H
Kosaki, R
Suzuki, T
Smith, R
Matsuo, N
机构：
[1] Keio Univ, Sch Med, Dept Pediat, Tokyo, Japan
[2] Niigata Univ, Sch Med, Dept Pediat, Niigata, Japan
[3] Keio Univ, Ctr Hlth, Tokyo, Japan
[4] Harvard Univ, Sch Med, Joslin Diabet Ctr, Boston, MA 02115 USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2000年 / 67卷 / 04期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
1932
引用
收藏
页码：347 / 347
页数：1
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