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	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.
	Fact Sheets for Health Professionals: Fragile X Syndrome: From the Victorian Government, Australia.
	Fragile X Association of Australia: Information on this disease, medical aspects, education, references, contacts and what's new in Australia
	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.
	Fragile X Research Foundation of Canada: Registered charity publishes a newsletter, invites applications for research grant, and explains how to donate or join.
	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.
	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.
	Living with Fragile X: One family's account of raising 3 children with Fragile X.
	Maryland Fragile X Resource Group: 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.
	Online Support Group: Support group for Family's who are dealing with Fragile X Syndrome.
	Pediatric Oncal: Information presented about Fragile X Syndrome, including the diagnoses and clinical manifestations.
	Queensland Fragile X Association: About QFXA, news, events, links and contacts. Also information of fragile X syndrome.
	The National Fragile X Foundation: Features information about the disease, its teatment, and inheritance.

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