A new cohort of MECP2 mutation screening in unexplained mental retardation:: Careful re-evaluation is the best indicator for molecular diagnosis

被引：11

作者：

Donzel-Javouhey, Anne

Thauvin-Robinet, Christel

Cusin, Veronica

Madinier, Nathalie

Manceau, Eric

Dipanda, Dominique

Dulieu, Veronique

Mugneret, Francine

Huet, Frederic

Teyssier, Jean-Raymond

Faivre, Laurence

机构：

[1] CHU Dijon, Dijon, France

[2] Fac Med, Dept Genet, Dijon, France

[3] CHU Dijon, Hop Enfants, Serv Pediat, Dijon, France

[4] CHU Dijon, Hop Enfants, Serv Pedopsychiat, Dijon, France

[5] CHU Dijon, Hop Enfants, Serv Reeducat Fonct, Dijon, France

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2006年 / 140A卷 / 14期

关键词：

D O I：

10.1002/ajmg.a.31314

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：1603 / 1607

页数：5

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