A severely affected male born into a Rett syndrome kindred supports X-linked inheritance and allows extension of the exclusion map

Am J Hum Genet. 1998 Jul;63(1):267-9. doi: 10.1086/301932.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Chromosome Mapping
  • Genetic Linkage / genetics*
  • Genotype
  • Haplotypes
  • Humans
  • Infant, Newborn
  • Male
  • Microsatellite Repeats / genetics
  • Pedigree
  • Rett Syndrome / etiology
  • Rett Syndrome / genetics*
  • X Chromosome / genetics*