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MeSH:( Steroid 21-hydroxylase)

2.The mutations caused steroid 21-hydroxylase deficiency on a patient with symptom of c-SW

Rita Bernhardt

Journal of Medical Research 2003;23(3):109-113

4.Three Cases of Congenital Adrenal Hyperplasia Owing to Multiple Mutations of CYP21 Gene.

Jun HEO ; Jae Hong YU ; Dong Ki JEONG

Journal of Korean Society of Pediatric Endocrinology 2001;6(2):176-181

5.Some mutations in CYP21 gene causing congenital adrenal hyperplasia due to 21-hydroxylase deficiency, the relationship between genotype phenotype and the carriers in family.

Hao Kiem Tran ; Phuong Thi Nguyen ; Lan Thi Thuong Vo

Journal of Medical Research 2007;55(6):109-116

6.A case of testicular adrenal rest tumor in a male child with congenital adrenal hyperplasia.

Joo Hwa KIM ; Kyong Ah YUN ; Choong Ho SHIN ; Sei Won YANG

Korean Journal of Pediatrics 2008;51(9):1018-1022

7.Analysis of CYP21A2 gene mutations among patients with classical steroid 21-hydroxylase deficiency.

Yueqing SU ; Hanqiang CHEN ; Wenbin ZHU ; Jing WANG ; Jinfu ZHOU ; Yao CHEN ; Hong ZHAO ; Yinglin ZENG ; Feng LIN ; Honghua ZHANG ; Qingying LIN

Chinese Journal of Medical Genetics 2016;33(6):786-791

8.A case of adrenocortical adenoma following long-term treatment in a patient with congenital adrenal hyperplasia.

Seung Rim LHO ; So Hyun PARK ; Min Ho JUNG ; Byung Churl LEE

Korean Journal of Pediatrics 2007;50(3):302-305

9.Analysis of clinical phenotypes and CYP21A2 gene variants in 18 patients with 21-hydroxylase deficiency.

Ruizhi ZHENG ; Li ZHANG ; Qian YUAN ; Hua MAN ; Junpeng YANG ; Yanfang WANG ; Ziying HU ; Huifeng ZHANG

Chinese Journal of Medical Genetics 2019;36(2):120-123

10.Genetic screening and prenatal diagnosis in 18 high-risk families with 21-hydroxylase deficiency.

Yanjie XIA ; Shiyue MEI ; Shuang HU ; Qinghua WU ; Xiangdong KONG

Chinese Journal of Medical Genetics 2019;36(2):103-107

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