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Williams Syndrome

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  • Williams Syndrome - Williams Syndrome is a rare neurodevelopmental disorder caused by a deletion of about 26 genes from the long arm of chromosome 7.
  • Williams Syndrome Association - The WSA is a resource for people and families living with Williams syndrome as well as doctors, researchers and educators.
  • Williams syndrome: MedlinePlus - Williams syndrome is a rare genetic disorder that can lead to problems with development.
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