Birth seasonality in Korean Prader-Willi syndrome with chromosome 15 microdeletion

PURPOSE: Prader-Willi syndrome (PWS) is a well-known genetic disorder, and microdeletion on chromosome 15 is the most common causal mechanism. Several previous studies have suggested that various environmental factors might be related to the pathogenesis of microdeletion in PWS. In this study, we in...

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Detalhes bibliográficos
Publicado no:Ann Pediatr Endocrinol Metab
Main Authors: Yang, Aram, Lee, Yeon Hee, Nam, Soon Young, Jeong, Yu Ju, Kyung, Yechan, Huh, Rimm, Lee, Jieun, Kwun, Younghee, Cho, Sung Yoon, Jin, Dong-Kyu
Formato: Artigo
Idioma:Inglês
Publicado em: The Korean Society of Pediatric Endocrinology 2015
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4397272/
https://ncbi.nlm.nih.gov/pubmed/25883926
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6065/apem.2015.20.1.40
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