Annals of Pediatric Endocrinology & Metabolism


An A627V-activating mutation in the thyroid-stimulating hormone receptor gene in familial nonautoimmune hyperthyroidism: Jung Hyun Shin, Go Hun Seo, Seung Hwan Oh, Woo Yeong Chung, Hye Young Kim, Young Mi Kim, Mi Hye Bae, Kyung Hee Park, Min Jung Kwak; Ann Pediatr Endocrinol Metab. 2020;25(4):282-286. Published online December 31, 2020; DOI: https://doi.org/10.6065/apem.2040076.038
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Clinical genetics of defects in thyroid hormone synthesis: Min Jung Kwak; Ann Pediatr Endocrinol Metab. 2018;23(4):169-175. Published online December 31, 2018; DOI: https://doi.org/10.6065/apem.2018.23.4.169
Web of Science 18 Crossref 18; Full text PubReader ePub PDF


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; DOI: https://doi.org/10.6065/apem.2017.22.3.203
Web of Science 3 Crossref 3; Full text PubReader ePub PDF


Guidelines for genetic skeletal dysplasias for pediatricians: Sung Yoon Cho, Dong-Kyu Jin; Ann Pediatr Endocrinol Metab. 2015;20(4):187-191. Published online December 31, 2015; DOI: https://doi.org/10.6065/apem.2015.20.4.187
Crossref 18; Full text PubReader ePub PDF

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