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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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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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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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Genotype of Steroid 21-Hydroxylase Gene and Clinical Characteristics in Patients with Congenital Adrenal Hyperplasia 21-Hydroxylase Deficiency.
Jung Min Ko, Jin Ho Choi, Gu Hwan Kim, Han Wook Yoo
Ann Pediatr Endocrinol Metab. 2005;10(1):57-63.
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Clinical and molecular characteristics of simple virilizing congenital adrenal hyperplasia due to 21-hydroxylase deficiency: insight from a tertiary pediatric center in Vietnam
Khanh Ngoc Nguyen, Giang Thi Kim Dang, Ngoc Thi Bich Can, Dien Minh Tran, Thao Phuong Bui, Mai Thi Phuong Nguyen, Huong Thu Pham, Ngoc Diem Ngo, Dung Chi Vu
Received November 13, 2024  Accepted April 4, 2025  
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