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European Journal of Pediatrics|March 30, 2010
Practical approach to steroid 5alpha-reductase type 2 deficiencyChong Kun CheonAnnals of Pediatric Endocrinology & Metabolism|October 26, 2016
Genetics of Prader-Willi syndrome and Prader-Will-Like syndromeChong Kun CheonKorean Journal of Pediatrics|October 12, 2018
Understanding of type 1 diabetes mellitus: what we know and where we goChong Kun CheonAmerican Journal of Medical Genetics. Part A|June 1, 2024
NANS-CDG: Expanding clinical insights with a novel patient with novel variantsSukdong Yoo, Chong Kun CheonKorean Journal of Pediatrics|October 30, 2015
Kabuki syndrome: clinical and molecular characteristicsChong-Kun Cheon, Jung Min KoKorean Journal of Pediatrics|October 18, 2014
Neurofibromatosis type 1: a single center's experience in KoreaMin Jeong Kim, Chong Kun CheonKorean Journal of Pediatrics|August 13, 2014
Prader-Willi syndrome: a single center's experience in KoreaYea Ji Kim, Chong Kun CheonAnnals of Pediatric Endocrinology & Metabolism|October 15, 2019
Evaluation and management of amenorrhea related to congenital sex hormonal disordersJu Young Yoon, Chong Kun CheonPediatrics International : Official Journal of the Japan Pediatric Society|September 23, 2020
Genotype and clinical outcomes in children with congenital adrenal hyperplasiaJu Young Yoon, Chong Kun CheonStem Cell Research|January 10, 2025
Human induced pluripotent stem cell line (PNUSCRi005-A) generated from severe type of Hunter syndrome patient carrying exonic deletion (exon 4-7 del) in in human iduronate 2-sulfatase geneNayeon Lee, Haneul Noh, Chong Kun CheonPageof 9