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X-inactivation and cytogenetic studies in a family with sensorineural hearing loss and Turner syndrome

✍ Scribed by NANCY SCULERATI; MARY ANN PERLE; CAROL ODDOUX; C.MARK CLAYTON; HARRY OSTRER

Book ID
117402471
Publisher
SAGE Publications
Year
1997
Tongue
English
Weight
811 KB
Volume
117
Category
Article
ISSN
0194-5998

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## Abstract Williams syndrome (WS) is a genetic neurodevelopmental disorder, most often accompanied by mild‐to‐moderate mental retardation. Individuals with WS show unique communication strengths and impairments that are challenging to treat in community, educational, and vocational settings. Many