RETT SYNDROME AND FRAGILE SITE IN Xp22

This publication has 4 references indexed in Scilit:

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• INFANTILE AUTISM AND RETT'S SYNDROME: COMMON CHROMOSOMAL DENOMINATOR
  The Lancet, 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
• On the frequency of telomeric chromosomal changes induced by culture conditions suitable for fragile X expression
  Human Genetics, 1982