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Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene
Ji-Hee Yoon, Soojin Hwang, Ja Hye Kim, Gu-Hwan Kim, Han-Wook Yoo, Jin-Ho Choi
Ann Pediatr Endocrinol Metab. 2024;29(1):54-59.   Published online February 29, 2024
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Clinical outcomes and genotype-phenotype correlations in patients with complete and partial androgen insensitivity syndromes
Nae-yun Lee, Ja Hye Kim, Ji-Hee Yoon, Soojin Hwang, Gu-Hwan Kim, Han-Wook Yoo, Jin-Ho Choi
Ann Pediatr Endocrinol Metab. 2023;28(3):184-192.   Published online February 1, 2023
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Molecular basis and genetic testing strategies for diagnosing 21-hydroxylase deficiency, including CAH-X syndrome
Ja Hye Kim, Gu-Hwan Kim, Han-Wook Yoo, Jin-Ho Choi
Ann Pediatr Endocrinol Metab. 2023;28(2):77-86.   Published online June 30, 2023
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Genotype-phenotype correlations and long-term efficacy of pamidronate therapy in patients with osteogenesis imperfecta
Yunha Choi, Soojin Hwang, Gu-Hwan Kim, Beom Hee Lee, Han-Wook Yoo, Jin-Ho Choi
Ann Pediatr Endocrinol Metab. 2022;27(1):22-29.   Published online January 25, 2022
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Clinical, endocrinological, and molecular features of four Korean cases of cytochrome P450 oxidoreductase deficiency
Yena Lee, Jin-Ho Choi, Arum Oh, Gu-Hwan Kim, Sook-Hyun Park, Jung Eun Moon, Cheol Woo Ko, Chong-Kun Cheon, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2020;25(2):97-103.   Published online June 30, 2020
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Long-term clinical outcome and the identification of homozygous CYP27B1 gene mutations in a patient with vitamin D hydroxylation-deficient rickets type 1A
Ja Hyang Cho, Eungu Kang, Gu-Hwan Kim, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2016;21(3):169-173.   Published online September 30, 2016
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Long-term efficacy of recombinant human growth hormone therapy in short-statured patients with Noonan syndrome
Insook Jeong, Eungu Kang, Ja Hyang Cho, Gu-Hwan Kim, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2016;21(1):26-30.   Published online March 31, 2016
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Endocrine dysfunctions in children with Williams-Beuren syndrome
Yoon-Myung Kim, Ja Hyang Cho, Eungu Kang, Gu-Hwan Kim, Eul-Ju Seo, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2016;21(1):15-20.   Published online March 31, 2016
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Recent advances in biochemical and molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Jin-Ho Choi, Gu-Hwan Kim, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2016;21(1):1-6.   Published online March 31, 2016
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Turner syndrome presented with tall stature due to overdosage of the SHOX gene
Go Hun Seo, Eungu Kang, Ja Hyang Cho, Beom Hee Lee, Jin-Ho Choi, Gu-Hwan Kim, Eul-Ju Seo, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2015;20(2):110-113.   Published online June 30, 2015
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Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience
Sun-Jeong Shin, Yeonah Sul, Ja Hye Kim, Ja Hyang Cho, Gu-Hwan Kim, Jae Hyun Kim, Jin-Ho Choi, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2015;20(1):27-33.   Published online March 31, 2015
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A novel de novo mutation within PHEX gene in a young girl with hypophosphatemic rickets and review of literature
Chong Kun Cheon, Hoon Sang Lee, Su Yung Kim, Min Jung Kwak, Gu-Hwan Kim, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2014;19(1):36-41.   Published online March 31, 2014
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p.R182C mutation in Korean twin with congenital lipoid adrenal hyperplasia
Hye Won Park, Byung Ok Kwak, Gu-Hwan Kim, Han-Wook Yoo, Sochung Chung
Ann Pediatr Endocrinol Metab. 2013;18(1):40-43.   Published online March 31, 2013
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