The prevalence of the FMR1 and FMR2 mutations among preschool children with language delay

This publication has 22 references indexed in Scilit:

• The FMR1 and FMR2 Mutations Are Not Common Etiologies of Academic Difficulty Among School-Age Children
  Journal of Developmental & Behavioral Pediatrics, 1997
• A simplified six item checklist for screening for fragile X syndrome in the pediatric population
  The Journal of Pediatrics, 1996
• Frequency and stability of the fragile X premutation
  Human Molecular Genetics, 1994
• Population studies of the fragile X: a molecular approach.
  Journal of Medical Genetics, 1993
• The effectiveness of early intervention: A critical review
  Journal of Paediatrics and Child Health, 1992
• Brief screening questionnaire for determining affected state in fragile X Syndrome: A consensus recommendation
  American Journal of Medical Genetics, 1992
• Effects of early intervention on cognitive function of low birth weight preterm infants
  The Journal of Pediatrics, 1992
• Detection of full fragile X mutation
  The Lancet, 1992
• Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
  Cell, 1991
• Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
  Published by Elsevier ,1991