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First published 2010-8

Mutational Analysis of the MECP2 Gene in Tunisian Patients With Rett Syndrome: A Novel Double Mutation

Nourhene Fendri-Kriaa, Emna Mkaouar-Rebai, Dorsaf Moalla [...]

Journal of Child Neurology

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First published 2008-01

X Chromosome Inactivation in Rett Syndrome and Its Correlations With MeCP2 Mutations and Phenotype

Xinhua Bao, Shengling Jiang, Fuying Song [...]

Journal of Child Neurology

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First published 2007-12

Rett Syndrome: Prevalence Among Chinese and a Comparison of MECP2 Mutations of Classic Rett Syndrome With Other Neurodevelopmental Disorders

Virginia C. N. Wong, Susanna Y. H. Li

Journal of Child Neurology

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Research article

First published 2002-03

Spectrum of MECP2 Mutations in Rett Syndrome

Thierry Bienvenu, Laurent Villard, Nicolas De Roux [...]

Genetic Testing and Molecular Biomarkers

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First published 2009-06

Methyl-CpG-binding Protein 2 (MECP2) Gene Mutations in an Italian Sample of Patients with Pervasive Developmental Disorder and Mental Retardation

Antonia Parmeggiani, Maria Rita Tedde, Annalisa Arbizzani [...]

Journal of Child Neurology

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Research article

First published 2008-09

Multiple De Novo Mutations in the MECP2 Gene

David J. Bunyan, David O. Robinson

Genetic Testing and Molecular Biomarkers

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Research article

First published 2009-02

A Novel MECP2 Gene Mutation in a Tunisian Patient with Rett Syndrome

Nourhène Fendri-Kriaa, Zaineb Abdelkafi, Imen Ben Rebeh [...]

Genetic Testing and Molecular Biomarkers

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First published 2002-01

Rett Syndrome: Clinical Manifestations in Males With MECP2 Mutations

Bruria Ben Zeev, Yuval Yaron, N. Carolyn Schanen [...]

Journal of Child Neurology

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Research article

First published 2009-02

A Multiplexed ARMS-PCR Approach for the Detection of Common MECP2 Mutations

Ibrahim Baris, Esra Battaloglu

Genetic Testing and Molecular Biomarkers

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First published 2004-12

Autonomic Dysfunction in Mental Retardation and Spastic Paraparesis With MECP2 Mutation

Maria Teresa Dotti, Francesca Guideri, Maurizio Acampa [...]

Journal of Child Neurology

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