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Williams Syndrome Learning Center
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Williams syndrome is a rare genetic disorder that can lead to problems with development.
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Williams syndrome is a genetic disorder caused by a deletion of a series of genes on chromosome 7q11. Individuals with Williams syndrome have distinctive facial features, mild mental retardation, heart and blood vessel problems, short stature, uni...
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Williams syndrome, first described in 1961, is a rare genetic condition with a wide array of clinical features.
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A rare genetic disorder first described by J.C.P. Williams of New Zealand, characterized by an abnormality on chromosome seven. Williams syndrome (WS) is a genetic disorder first described by J.C.P. Williams of New Zealand. It is estimated to occu...
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Williams syndrome is a genetic disorder caused by a deletion of a series of genes on chromosome 7q11. Individuals with Williams syndrome have distinctive facial features, mild mental retardation, heart and blood vessel problems, short stature, uni...
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