Links To Fragile X Sites

FRAXA: Founded by parents in 1994, FRAXA is a national non-profit parent run organization, which funds medical research aimed at finding a specific treatment for Fragile X.
The National Fragile X Foundation: The Home Page of the National Fragile X Foundation. Located out of Denver, Colorado, the Foundation is major support and resource center for Fragile X families.
Genecare: Genecare's listing of several Fragile X publications, including Dr. Marcia Braden's Fragile: Handle with Care
Fragile X Photo Gallery: These children have fragile X syndrome. If you look closely, you may notice large ears, slightly elongated faces, and prominent foreheads. However, it would be tough to pick these kids out of a crowd!
Fragile X listserv: A listserv for Fragile X information