Wectar - Health - Conditions and Diseases - Genetic Disorders - Fragile X Syndrome

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	Fragile X Research Foundation of Canada URL: http://www.fragile-x.ca/ ODP description: Funds investigation of the most common inherited form of mental impairment and developmental disability, and provides newsletters and discussion groups, invites applications for research grants, and explains how to donate or join. Page title: Movie1
	Living with Fragile X URL: http://fragilex.ca ODP description: One family's account of raising 3 children with Fragile X. Page title: fragilex.ca home page Page description: This page details the trial and tribulations of raising three children with Fragile X.
	FRAXA Research Foundation Home Page URL: http://www.fraxa.org/ ODP description: Non-profit organization run by parents. Fighting to find a cure for Fragile X Syndrome and helping Fragile X Family's. Page title: FRAXA - Fragile X Research Foundation
	Conquer Fragile X, Inc. URL: http://www.conquerfragilex.org ODP description: Creating a virtual research center in Israel to find a cure. Page title: Fragile X - Fragile X Syndrome - Mental Retardation - Genetic Defects - Autism - Learning Disabilities - Medical Research In Israel Page description: Fragile X is the leading inherited cause of mental retardation. This site creates a virtual research center in Israel for the research and cure of Fragile X.
	Pediatric Oncal URL: http://www.pediatriconcall.com/fordoctor/diseasesandcondition/fragile_x.asp ODP description: Information presented about Fragile X Syndrome, including the diagnoses and clinical manifestations. Page title: Fragile X Syndrome Pediatric Oncall Page description: Fragile X Syndrome Pediatric Oncall
	Fragile X Association of Australia URL: http://www.fragilex.org.au/ ODP description: Information on this disease, medical aspects, education, references, contacts and what's new in Australia Page title: Fragile X
	Fragile X Syndrome - Diagnostic and Carrier Testing URL: http://www.faseb.org/genetics/acmg/pol-16.htm ODP description: A Policy Statement from the American College of Medical Genetics. Page title: Fragile X Syndrome
	Maryland Fragile X Resource Group URL: http://www.mdfragilex.org/ ODP description: 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. Page description: The Maryland Fragile X Resource Group is a group of families in the MD/DC area who have children affected with Fragile X Syndrome. We are a very active group that supports education, promotes awareness and funds research on Fragile X.
	Online Support Group URL: http://groups.yahoo.com/group/fragilex/ ODP description: Support group for Family's who are dealing with Fragile X Syndrome. Page title: fragilex : This is a forum for parents and family members of children who have fragile x syndrome, to share and help eachother through. On Page description: fragilex: This is a forum for parents and family members of children who have fragile x syndrome, to share and help eachother through. On
	Fragile X Association of Southern California URL: http://www.fraxsocal.org ODP description: 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. Page title: What is Fragile X? Page description: Fragile X Association of Southern California promotes public awareness of Fragile X syndrome with emphasis on Educatiors and Health Professionals and also supports scientific research.
	The National Fragile X Foundation URL: http://www.fragilex.org/ ODP description: Features information about the disease, its treatment, and inheritance. Page title: The National Fragile X Foundation - Fragile X Syndrome
	Carolina Fragile X Project URL: http://www.fpg.unc.edu/~fx/ ODP description: A series of studies examining the impact of fragile X syndrome (FXS) on individuals, families and the agencies that serve them.