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Prader-Willi syndrome: a single center's experience in Korea

PURPOSE: Prader-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) trea...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Kim, Yea Ji, Cheon, Chong Kun
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: The Korean Pediatric Society 2014
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4127393/
https://ncbi.nlm.nih.gov/pubmed/25114691
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3345/kjp.2014.57.7.310
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