| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10448497 | Journal of Communication Disorders | 2005 | 14 Pages |
Abstract
The reader will obtain information about: (1) the genetic inheritance patterns and clinical characteristics of Prader-Willi Syndrome, (2) genotypic/phenotypic relationships specific to Prader-Willi Syndrome, and (3) clinical implications, management, and outcomes in a case description of a child with PWS due to maternal uniparental disomy inheritance pattern.
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Authors
Monica L. Bellon-Harn,