A series of studies examining the impact of fragile X syndrome (FXS) on individuals, families and the agencies that serve them.

Creating a virtual research center in Israel to find a cure.

From the Victorian Government, Australia.

Information on this disease, medical aspects, education, references, contacts and what's new in Australia

Fragile X Syndrome is the leading inherited cause of developmental disabilities and mental impairment worldwide. It affects 1 in 2,000 males and 1 in 4,000 females. It is estimated that 1 in 259 females are carries of the premutation.

Describing Fragile X Syndrome.

Registered charity publishes a newsletter, invites applications for research grant, and explains how to donate or join.

Single page on recognition of the condition in young children.

A Policy Statement from the American College of Medical Genetics.

Non-profit organization run by parents. Fighting to find a cure for Fragile X Syndrome and helping Fragile X Family's.

One family's account of raising 3 children with Fragile X.

A community of families in and around the Washington-Baltimore metro area that have children affected by Fragile X Syndrome. Includes news, upcoming events, and resources.

Support group for Family's who are dealing with Fragile X Syndrome.

Information presented about Fragile X Syndrome, including the diagnoses and clinical manifestations.

About QFXA, news, events, links and contacts. Also information of fragile X syndrome.

Features information about the disease, its teatment, and inheritance.