A novel mutation in the MSX2 homeobox gene of a family with foramina parietalia permagna, headache and vascular anomaly

被引：5
|
作者：
Ghassibe, Michella
Bernier, Vincent
Boon, Laurence M.
Vikkula, Miikka
机构：
[1] Christian Duve Inst Cellular Pathol, Lab Human Mol Genet, B-1200 Brussels, Belgium
[2] Univ Catholique Louvain, B-1200 Brussels, Belgium
[3] Ctr Hosp Chretiens, Dept Pediat, Liege, Belgium
[4] Univ Catholique Louvain, Ctr Vasc Anomalies, Div Plast Surg, B-1200 Brussels, Belgium
来源：
EUROPEAN JOURNAL OF PEDIATRICS | 2006年 / 165卷 / 10期
关键词：
D O I：
10.1007/s00431-006-0138-8
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
[No abstract available]
引用
收藏
页码：734 / 735
页数：2
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