Prader-Willi syndrome: a single center's experience in Korea
PurposePrader-Willi syndrome (PWS) is a complex genetic disorder that results from the lack of paternally expressed genes in the chromosome 15q11-q13 region. This study was performed to delineate the clinical features of PWS infants and toddlers and the effects of two-year growth hormone (GH) treatm...
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| Main Authors: | , |
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| Format: | Book |
| Published: |
Korean Pediatric Society,
2014-07-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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