Analysis of the parental origin of de novo MECP2 mutations and X chromosome inactivation in fifteen sporadic cases with Rett syndrome

von Zhu, Xing-wang
Veröffentlicht in: Zhonghua er ke za zhi = Chinese journal of pediatrics (2009)

Correlation between MECP2 genotype and phenotype in Chinese patients with Rett syndrome

von Li, Mei-rong
Veröffentlicht in: Zhonghua er ke za zhi = Chinese journal of pediatrics (2009)

X chromosome inactivation patterns in patients with Rett syndrome and their mothers and the parental origin of the priority inactive X chromosome

von Jiang, Sheng-ling
Veröffentlicht in: Zhonghua er ke za zhi = Chinese journal of pediatrics (2006)

MECP2 gene mutations in twenty-six cases with atypical Rett syndrome

von Li, Mei-rong
Veröffentlicht in: Zhonghua er ke za zhi = Chinese journal of pediatrics (2006)