

![]() |
Williams syndrome is a rare genetic disorder that can lead to problems with development.
|
|
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...
|
|
|
Williams syndrome, first described in 1961, is a rare genetic condition with a wide array of clinical features.
|
|
|
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...
|
|
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...
|


