Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations

This publication has 17 references indexed in Scilit:

• A de novo X; 3 translocation in Rett syndrome
  American Journal of Medical Genetics, 1990
• Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 622-643
  Cytogenetic and Genome Research, 1989
• Report of the committee on the genetic constitution of the X chromosome
  Cytogenetic and Genome Research, 1988
• The genetics of rett syndrome: The consequences of a disorder where every case is a new mutation
  American Journal of Medical Genetics, 1986
• Rett syndrome: Lack of association with fragile site Xp22 and strategy for genetic mapping of X-linked new mutations
  American Journal of Medical Genetics, 1986
• Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids.
  1985
• The clinical pattern of the rett syndrome
  Brain & Development, 1985
• A simple method for fusing human lymphocytes with rodent cells in monolayer by polyethylene glycol
  Somatic Cell and Molecular Genetics, 1981
• Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.
  Proceedings of the National Academy of Sciences, 1977
• A CONTRIBUTION TO GENETICS OF INCONTINENTIA PIGMENTI
  1961