Screening of MECP2 coding sequence in patients with phenotypes of decreasing likelihood for Rett syndrome:: a cohort of 171 cases -: art. no. e85

被引：35

作者：

Kammoun, F

de Roux, N

Boespflug-Tanguy, O

Vallée, L

Seng, R

Tardieu, M

Landrieu, P ^{[1
]}

机构：

[1] CHU Bicetre, Serv Neurol Pediat, F-94275 Le Kremlin Bicetre, France

[2] CHU Bicetre, Lab Hormonol & Biol Mol, F-94275 Le Kremlin Bicetre, France

[3] CHU Clermont Ferrand, Serv Neuropediat, F-63003 Clermont Ferrand 1, France

[4] Ctr Hosp Reg & Univ Lille, Hop Roger Salengro, Serv Neuropediat, F-59037 Lille, France

[5] CHU Bicetre, Serv Epidemiol & Sante Publ, F-94275 Le Kremlin Bicetre, France

来源：

JOURNAL OF MEDICAL GENETICS | 2004年 / 41卷 / 06期

关键词：

D O I：

10.1136/jmg.2003.014480

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页数：7

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