Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome -: art. no. e12

被引：182

作者：

Meins, M

Lehmann, J

Gerresheim, F

Herchenbach, J

Hagedorn, M

Hameister, K

Epplen, JT

机构：

[1] Ruhr Univ Bochum, Dept Human Genet, D-44801 Bochum, Germany

[2] Fachklin Kinderneurol & Sozialpaediat Konigsborn, Unna, Germany

来源：

JOURNAL OF MEDICAL GENETICS | 2005年 / 42卷 / 02期

关键词：

D O I：

10.1136/jmg.2004.023804

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页数：6

共 29 条

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