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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...

詳細記述

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書誌詳細
出版年:Ann Pediatr Endocrinol Metab
主要な著者: 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
フォーマット: Artigo
言語:Inglês
出版事項: The Korean Society of Pediatric Endocrinology 2015
主題:
オンライン・アクセス: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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