Autism: the point of view from fragile X studies.

This publication has 83 references indexed in Scilit:

• High functioning fragile X males: Demonstration of an unmethylated fully expanded FMR‐1 mutation associated with protein expression
  American Journal of Medical Genetics, 1994
• Molecular‐neurobehavioral associations in females with the fragile X full mutation
  American Journal of Medical Genetics, 1994
• High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome
  Human Molecular Genetics, 1993
• Trajectory of adaptive behavior in males with fragile X syndrome
  Journal of Autism and Developmental Disorders, 1993
• Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndrome
  Nature Genetics, 1993
• A recombination–based assay demonstrates that the fragile X sequence is transcribed widely during development
  Nature Genetics, 1993
• Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
  Cell, 1991
• Absence of expression of the FMR-1 gene in fragile X syndrome
  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
• Cerebellar Hypoplasia and Autism
  New England Journal of Medicine, 1988