Elevated expression of MeCP2 in cardiac and skeletal tissues is detrimental for normal development

Mecp2 deficiency decreases bone formation and reduces bone volume in a rodent model of Rett syndrome

(2009) R.D. O'Connor et al.   BONE

The clinical variability of theMECP2duplication syndrome: description of two families with duplications excludingL1CAMandFLNA

(2009)   CLINICAL GENETICS

Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching

(2009) Claudia M.B. Carvalho et al.   HUMAN MOLECULAR GENETICS

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

(2009) Antonia Parmeggiani et al.   JOURNAL OF CHILD NEUROLOGY

Distal Xq duplication and functional Xq disomy

(2009) Damien Sanlaville et al.   Orphanet Journal of Rare Diseases

Neurologic Aspects of MECP2 Gene Duplication in Male Patients

(2009) Bernard Echenne et al.   PEDIATRIC NEUROLOGY

Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice

(2009) Daniela Tropea et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy

(2008) Dorien Lugtenberg et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A novel hypomorphic MECP2 point mutation is associated with a neuropsychiatric phenotype

(2008) Abidemi A. Adegbola et al.   HUMAN GENETICS

MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription

(2008) M. Chahrour et al.   SCIENCE