PTPN11 mutation in a young man with Noonan syndrome and Retinitis Pigmentosa

被引：0
|
作者：
Schollen, E [1 ]
Matthijs, G [1 ]
Fryns, JF [1 ]
机构：
[1] Catholic Univ Louvain, Ctr Human Genet, B-3000 Louvain, Belgium
来源：
GENETIC COUNSELING | 2003年 / 14卷 / 02期
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D O I：
暂无
中图分类号：
Q81 [生物工程学（生物技术）]; Q93 [微生物学];
学科分类号：
071005 ; 0836 ; 090102 ; 100705 ;
摘要：
引用
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页码：259 / 259
页数：1
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