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Original Articles
Molecular Genetic Studies on the Human CYP21A2 Gene (1).
Byung Kiu Park, Hyang Ok Woo, Han Wook Woo
Endocrinol Metab. 1994;9(3):219-227.   Published online November 6, 2019
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Six Cases of Congenital Adrenal Hyperplasia That Were Due to 17alpha-hydroxylase/17,20-lyase Deficiency.
Dong Hoon Shin, Sung Hoon Yu, Young Min Choi et al.
Endocrinol Metab. 2009;24(2):109-115.   Published online June 1, 2009
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Case Reports
A Case of Congenital Adrenal Hyperplasia Combined with a Testicular Adrenal Rest Tumor and Adrenal Incidentaloma.
Gyu Rang Cho, Hee Won Chueh, Jung Pyo Kim et al.
Endocrinol Metab. 2007;22(5):365-370.   Published online October 1, 2007
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Two Cases of Simple Virilizing Congenital Adrenal Hyperplasia with Compound Heterozygous Mutations of CYP21 Gene.
Koon Soon Kim, Yun Sun Choi, Youn Sun Bai, So Young Rha, Young Suk Jo, Minho Shong
Endocrinol Metab. 2007;22(4):299-304.   Published online August 1, 2007
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A Case of Congenital Adrenal Hyperplasia due to 11beta-Hydroxylase Deficiency.
Ohk Hyun Ryu, Hye Jin Yoo, Soo Yeon Park et al.
Endocrinol Metab. 2004;19(1):58-63.   Published online February 1, 2004
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A Case of Primary Amenorrhea due to 17 -Hydroxylase Deficiency.
Hong Seub Rim, Seon Hwa Lee, Jung Min Hong et al.
Endocrinol Metab. 2001;16(1):130-133.   Published online February 1, 2001
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Original Articles
A Study on the Relationship Between Genotype and Phenotype in Korean Patients with Congenital Adrenogenital Syndrome Caused by 21-hydroxylase Deficiency.
Dong Kyu Jin, Jung Sim Kim, Seung Mi Song et al.
Endocrinol Metab. 2000;15(2):237-247.   Published online January 1, 2001
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Endocrinology
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