Mutations in the MECP2 gene in a cohort of girls with Rett syndrome

J Med Genet. 2000 Aug;37(8):610-2. doi: 10.1136/jmg.37.8.610.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child
  • Child, Preschool
  • Chromosomes, Human, Pair 1*
  • Chromosomes, Human, Pair 15*
  • Epilepsy / genetics
  • Female
  • Growth Disorders / genetics
  • Humans
  • Intellectual Disability / genetics
  • Monosomy*
  • Translocation, Genetic*
  • Trisomy*