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A case of de novo 18p deletion syndrome with panhypopituitarism
Aram Yang, Jinsup Kim, Sung Yoon Cho, Ji-Eun Lee, Hee-Jin Kim, Dong-Kyu Jin
Ann Pediatr Endocrinol Metab. 2019;24(1):60-63.   Published online March 31, 2019
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A novel de novo mosaic mutation in PHEX in a Korean patient with hypophosphatemic rickets
Misun Yang, Jinsup Kim, Aram Yang, Jahyun Jang, Tae Yeon Jeon, Sung Yoon Cho, Dong-Kyu Jin
Ann Pediatr Endocrinol Metab. 2018;23(4):229-234.   Published online December 31, 2018
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Etiological trends in male central precocious puberty
Jisun Lee, Jinsup Kim, Aram Yang, Sung Yoon Cho, Dong-Kyu Jin
Ann Pediatr Endocrinol Metab. 2018;23(2):75-80.   Published online June 20, 2018
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An atypical case of Noonan syndrome with KRAS mutation diagnosed by targeted exome sequencing
Jinsup Kim, Sung Yoon Cho, Aram Yang, Ja-Hyun Jang, Youngbin Choi, Ji-Eun Lee, Dong-Kyu Jin
Ann Pediatr Endocrinol Metab. 2017;22(3):203-207.   Published online September 28, 2017
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2q37 Deletion syndrome confirmed by high-resolution cytogenetic analysis
Eun-Kyung Cho, Jinsup Kim, Aram Yang, Sung Yoon Cho, Dong-Kyu Jin
Ann Pediatr Endocrinol Metab. 2017;22(2):129-132.   Published online June 28, 2017
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Birth seasonality in Korean Prader-Willi syndrome with chromosome 15 microdeletion
Aram Yang, Yeon Hee Lee, Soon Young Nam, Yu Ju Jeong, Yechan Kyung, Rimm Huh, Jieun Lee, Younghee Kwun, Sung Yoon Cho, Dong-Kyu Jin
Ann Pediatr Endocrinol Metab. 2015;20(1):40-45.   Published online March 31, 2015
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