Systematic review of the clinical and genetic aspects of Prader-Willi syndrome

Prader-Willi syndrome (PWS) is a complex multisystem genetic disorder that is caused by the lack of expression of paternally inherited imprinted genes on chromosome 15q11-q13. This syndrome has a characteristic phenotype including severe neonatal hypotonia, early-onset hyperphagia, development of mo...

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Prif Awdur: Dong Kyu Jin (Awdur)
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Cyhoeddwyd: Korean Pediatric Society, 2011-02-01T00:00:00Z.
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3rd Floor Main Library

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