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| Web Pages |
| Fragile X Association of Southern California |
| 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. |
| FRAXA Research Foundation Home Page |
| Non-profit organization run by parents. Fighting to find a cure for Fragile X Syndrome and helping Fragile X Family's. |
| The National Fragile X Foundation |
| The National Fragile X Foundation informes and educates about the Fragile X Syndrome. |
| Familyvillage |
| Links to places to talk about Fragile X. |
| Fragile X Syndrome - Diagnostic and Carrier Testing |
| A Policy Statement from the American College of Medical Genetics. |
| Fragile X Syndrome |
| Single page on recognition of the condition in young children. |
| Fragile X Fact's Page |
| Describing Fragile X Syndrome. |
| Fragile X Association of Australia |
| Information on this disease, medical aspects, education, references, contacts and what's new in Australia |
| Carolina Fragile X Project |
| A series of studies examining the impact of fragile X syndrome (FXS) on individuals, families and the agencies that serve them. |
| Conquer Fragile X, Inc. |
| Creating a virtual research center in Israel to find a cure. |
| Queensland Fragile X Association |
| About QFXA, news, events, links and contacts. Also information of fragile X syndrome. |
| Online Support Group |
| Support group for Family's who are dealing with Fragile X Syndrome. |
| Fact Sheets for Health Professionals: Fragile X Syndrome |
| From the Victorian Government, Australia. |
| Living with Fragile X |
| A families acount of raising 3 children with Fragile X. |