Hereditary haemorrhagic telangiectasia - the different phenotypes caused by endoglin and ALK1 mutation

被引：0
|
作者：
Berg, J
Marchuk, D
Guttmacher, A
Porteous, M
机构：
[1] Univ Edinburgh, Human Genet Unit, Edinburgh EH8 9YL, Midlothian, Scotland
[2] Duke Univ, Dept Genet, Durham, NC 27706 USA
来源：
JOURNAL OF MEDICAL GENETICS | 1999年 / 36卷
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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：
引用
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页码：S29 / S29
页数：1
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