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- Genetic aspects of type 1 diabetes
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Hae Sang Lee
, Jin Soon Hwang - Ann Pediatr Endocrinol Metab. 2019;24(3):143-148. Published online September 30, 2019
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- Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a mutation in the arginine-vasopressin II gene in four generations of a Korean family
- Myo-Jing Kim, Young-Eun Kim, Chang-Seok Ki, Jae-Ho Yoo
- Ann Pediatr Endocrinol Metab. 2014;19(4):220-224. Published online December 31, 2014
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- Genotype-phenotype correlation in 27 pediatric patients in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a single center
- Yangho Yoo, Mi Sun Chang, Jieun Lee, Sung Yoon Cho, Sung Won Park, Dong-Kyu Jin, Hyung-Doo Park
- Ann Pediatr Endocrinol Metab. 2013;18(3):128-134. Published online September 30, 2013
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- A Single-Arm, Phase III Study to Assess Efficacy and Safety after 6-Month-Treatment of Eutropin(TM) Inj. (Recombinant Human Growth Hormone) in Prepubertal Children with Short Stature due to Small for Gestational Age.
- Kee Hyoung Lee, Byung Churl Lee, Cheol Woo Ko, Dong Kyu Jin, Sei Won Yang, Han Wook Yoo, Woo Yeong Chung, Duk Hee Kim, Byung Kyu Suh
- Ann Pediatr Endocrinol Metab. 2011;16(3):157-164.
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- A Korean child with DICER1 syndrome presenting with thyroid manifestations accompanied by other types of neoplasms: case report with a review of literatures
- Minji Kim, Jun Lee, Sukdong Yoo, Ji Yeon Song, Eu Jeen Yang, Seong Heon Kim, Chong Kun Cheon, Ju Young Yoon
- Received August 27, 2022 Accepted October 27, 2022
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DOI: https://doi.org/10.6065/apem.2244206.103 [Accepted]
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