X chromosome inactivation patterns in brain in Rett syndrome: implications for the disease phenotype

This publication has 28 references indexed in Scilit:

• Associations between meCP2 mutations, x‐chromosome inactivation, and phenotype
  Mental Retardation and Developmental Disabilities Research Reviews, 2002
• Rett syndrome: clinical characteristics and recent genetic advances
  Disability and Rehabilitation, 2001
• Rett syndrome: a surprising result of mutation in MECP2
  Human Molecular Genetics, 2000
• Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome
  Journal of Medical Genetics, 2000
• Mutations in the MECP2 gene in a cohort of girls with Rett syndrome
  Journal of Medical Genetics, 2000
• Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients.
  Human Molecular Genetics, 2000
• MECP2 mutations account for most cases of typical forms of Rett syndrome
  Human Molecular Genetics, 2000
• Rett syndrome: Methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations
  American Journal of Medical Genetics, 2000
• Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG Hotspots
  American Journal of Human Genetics, 1999
• Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
  Nature Genetics, 1999