Associated Papers
Analysis of the parental origin of de novo MECP2 mutations and X chromosome inactivation in 24 sporadic patients with Rett syndrome in China.
Zhu X et al.
Journal of Child Neurology, 2010
[Analysis of the parental origin of de novo MECP2 mutations and X chromosome inactivation in fifteen sporadic cases with Rett syndrome].
Zhu XW et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2009
[Methyl-CpG-binding protein 2 gene and CDKL5 gene mutation in patients with Rett syndrome: analysis of 177 Chinese pediatric patients].
Li MR et al.
Zhonghua Yi Xue Za Zhi, 2009
[Correlation between MECP2 genotype and phenotype in Chinese patients with Rett syndrome].
Li MR et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2009
MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome.
Li MR et al.
Journal of Human Genetics, 2007
[X chromosome inactivation patterns in patients with Rett syndrome and their mothers and the parental origin of the priority inactive X chromosome].
Jiang SL et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2006
[MECP2 gene mutations in twenty-six cases with atypical Rett syndrome].
Li MR et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2006
[Clinical feature of Rett syndrome and MeCP2 genotype/phenotype correlation analysis].
Bao XH et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2004
MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features.
Auranen M et al.
Neurology, 2001
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