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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; Harry Ostrer

Book ID
117400868
Publisher
SAGE Publications
Year
1995
Tongue
English
Weight
110 KB
Volume
113
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