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

Zhonghua er ke za zhi. Chinese journal of pediatrics

Volumn 47, Issue 8, 2009, Pages 565-569

  Zhu, Xing wang ^a   Pan, Hong ^b   Li, Mei rong ^b   Bao, Xin hua ^b   Zhang, Jing jing ^b   Wu, Xi ru ^b  

^a PEKING UNIVERSITY FIRST HOSPITAL   (China)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

METHYL CPG BINDING PROTEIN 2;

ARTICLE; CHROMOSOME ABERRATION; FEMALE; GENETICS; HUMAN; MALE; MUTATION; RETT SYNDROME; SINGLE NUCLEOTIDE POLYMORPHISM; X CHROMOSOME; X CHROMOSOME INACTIVATION;

CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, X; FEMALE; HUMANS; MALE; METHYL-CPG-BINDING PROTEIN 2; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; RETT SYNDROME; X CHROMOSOME INACTIVATION;

EID: 79951972628     PISSN: 05781310     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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