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
收藏
页数：7
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