The Fragile X Alliance Inc is a non-profit organisation whose mission statement is to promote education and research as well as disseminate information and new findings about fragile X syndrome. 

The Fragile X Alliance Clinic was established in April 1998 to meet the specific needs of affected individuals, their families and thre carers. We have now seen over 400 children and adults of all ages with either the full or premutation throughout Australia & New Zealand.