Related references
Note: Only part of the references are listed.Early-onset seizure variant of Rett syndrome: Definition of the clinical diagnostic criteria
R. Artuso et al.
BRAIN & DEVELOPMENT (2010)
Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant)
A. Renieri et al.
BRAIN & DEVELOPMENT (2009)
FOXG1 is responsible for the congenital variant of Rett syndrome
Francesca Ariani et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Key clinical features to identify girls with CDKL5 mutations
Nadia Bahi-Buisson et al.
BRAIN (2008)
Specific mutations in Methyl-CpG-Binding Protein 2 confer different severity in Rett syndrome
J. L. Neul et al.
NEUROLOGY (2008)
Rett syndrome: North American database
Alan K. Percy et al.
JOURNAL OF CHILD NEUROLOGY (2007)
CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients
H. L. Archer et al.
JOURNAL OF MEDICAL GENETICS (2006)
Early progressive encephalopathy in boys and MECP2 mutations
P. Kankirawatana et al.
NEUROLOGY (2006)
Abnormal general movements in girls with Rett disorder: The first four months of life
C Einspieler et al.
BRAIN & DEVELOPMENT (2005)
Trisomy 21 and Rett syndrome:: A double burden
H Leonard et al.
JOURNAL OF PAEDIATRICS AND CHILD HEALTH (2004)
Identification of MeCP2 mutations in a series of females with autistic disorder
RM Carney et al.
PEDIATRIC NEUROLOGY (2003)
Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein
P Watson et al.
JOURNAL OF MEDICAL GENETICS (2001)
Rett syndrome:: analysis of MECP2 and clinical characterization of 31 patients
P Huppke et al.
HUMAN MOLECULAR GENETICS (2000)
Share Paper
