Re-evaluation of MRX36 family after discovery of an ARX gene mutation reveals mild neurological features of Partington syndrome

被引：26

作者：

Frints, SGM ^{[1
]}

Froyen, G

Marynen, P

Willekens, D

Legius, E

Fryns, JP

机构：

[1] Univ Hosp Leuven, Clin Genet Unit, Dept Human Genet, Herestr 49, B-3000 Louvain, Belgium

[2] Univ Leuven VIB, Dept Human Genet, Human Genome Lab, Louvain, Belgium

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 2002年 / 112卷 / 04期

关键词：

D O I：

10.1002/ajmg.10629

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：427 / 428

页数：2

共 5 条

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[3] 2-5
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