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- Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene
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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
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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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- The Behavioral and Psychic Masculinizing Scores and Its Related Factors in Female Patients with Congenital Adrenal Hyperplasia Caused by 21-Hydroxylase Deficiency.
- Il Tae Hwang, Seong Gon Ryu, Kyung Hee Yi
- Ann Pediatr Endocrinol Metab. 2005;10(1):64-70.
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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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