Linkage analysis of the Rett syndrome using human chromosomal specific probes

This publication has 13 references indexed in Scilit:

• Detection of specific sequences among DNA fragments separated by gel electrophoresis
  Published by Elsevier ,2006
• Rett's Syndrome: Prevalence and Impact on Progressive Severe Mental Retardation in Girls
  Acta Paediatrica, 1985
• Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms.
  Proceedings of the National Academy of Sciences, 1984
• Evidence for integrated EBV genomes in Raji cellular DNA
  Nucleic Acids Research, 1984
• A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: Report of 35 cases
  Annals of Neurology, 1983
• Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome
  Nucleic Acids Research, 1983
• The mendelian inheritance of a human X chromosome-specific DNA sequence polymorphism and its use in linkage studies of genetic disease
  Human Genetics, 1982
• Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation.
  Proceedings of the National Academy of Sciences, 1978
• Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I
  Journal of Molecular Biology, 1977
• The determination of the molecular weight of ribonucleic acid by polyacrylamide-gel electrophoresis. The effects of changes in conformation
  Biochemical Journal, 1969