Genotype and early development in Rett syndrome: The value of international data

Brain and Development

Volumn 27, Issue SUPPL. 1, 2005, Pages

  Leonard, Helen ^a   Moore, Hannah ^a   Carey, Mary ^a   Fyfe, Susan ^b   Hall, Sonj ^c   Robertson, Laila ^a   Xi, Ru Wu ^d   Bao, Xinhua ^d   Pan, Hong ^d   Christodoulou, John ^e,f   Williamson, Sarah ^e,f   De Klerk, Nick ^a  

^a UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^b CURTIN UNIVERSITY   (Australia)

^c UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^d PEKING UNIVERSITY FIRST HOSPITAL   (China)

^e UNIVERSITY OF SYDNEY   (Australia)

^f CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

Author keywords

Database; Early development; International; Internet; MECP2; Phenotype; Rett syndrome

Indexed keywords

METHYL CPG BINDING PROTEIN 2;

BEHAVIOR DISORDER; COMPUTER NETWORK; CONFERENCE PAPER; DEVELOPMENTAL DISORDER; DEVELOPMENTAL GENETICS; DISEASE COURSE; DISEASE SEVERITY; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; MOTOR DYSFUNCTION; MUTATIONAL ANALYSIS; PERINATAL PERIOD; PREVALENCE; RETT SYNDROME; SCORING SYSTEM; SEX RATIO; STATISTICAL SIGNIFICANCE;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; DATABASES, FACTUAL; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; GENOTYPE; HUMANS; INFANT; INTERNATIONALITY; METHYL-CPG-BINDING PROTEIN 2; MUTATION; RETROSPECTIVE STUDIES; RETT SYNDROME;

EID: 27144502649     PISSN: 03877604     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.braindev.2005.03.023     Document Type: Conference Paper

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