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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Ann Pediatr Endocrinol Metab
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: The Korean Society of Pediatric Endocrinology 2015
Pynciau:
Original Article
Mynediad Ar-lein: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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