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Williams Syndrome Websites

Williams syndrome is a rare neurodevelopmental disorder caused by a deletion of about 26 genes from the long arm of chromosome 7. It is characterized by mental disability, heart defects and unusual facial features.- Category ID : 76429
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NORD : Williams Syndrome

Offers alternative names, a general discussion and resources.
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Williams Syndrome

Information sheet compiled by NINDS, the National Institute of Neurological Disorders and Stroke.
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Wikipedia: Williams Syndrome

A concise summary of its cause and symptoms.
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Williams Syndrome (WMS, WS)

National Library of Medicine provides a list of synonyms, a summary of the syndrome, and major physical features.
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A Music Camp for Those Afflicted but Gifted, Too

New York Times feature article about the Belvoir Terrace summer music camp program for people with Williams syndrome.
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