Rett syndrome: confirmation of X-linked dominant inheritance, and localization of the gene to Xq28

Am J Hum Genet. 1998 Nov;63(5):1552-8. doi: 10.1086/302105.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Brazil
  • Child
  • Child, Preschool
  • Chromosome Mapping
  • Female
  • Genes, Dominant*
  • Genetic Markers
  • Genotype
  • Humans
  • Male
  • Nuclear Family
  • Pedigree
  • Rett Syndrome / genetics*
  • X Chromosome*

Substances

  • Genetic Markers