1.
Molecular Genetic Analysis of Chinese Families with 21-Hydroxylase Deficiency;
21-羟化酶缺乏症家系的基因突变研究
2.
Nursing care of children with salt wasting phenotype of 21-hydroxylase deficiency
21-羟化酶缺乏失盐型患儿的护理
3.
hydroxylase deficiency
１７α－羟化酶缺乏症
4.
21-hydroxylase deficiency
２１－羟化酶缺乏症
5.
Follow-Up on Puberty Development and Final Height in 41 Children with Simple Virilizing Form of 21-Hydroxylase Deficiency
单纯男性化型21羟化酶缺乏症患儿41例青春发育与最终身高随访
6.
hydroxysteroid oxidoreductase deficiency
１７β－羟类固醇氧化还原酶缺乏症
7.
Right adrenal "tumor-like" hyperplasia in an adult with 21-hydroxylase deficiency-a case report.
21-羟化酶缺陷症伴右肾上腺“瘤样”增生1例
8.
18-oxylase deficiency
１８－氧化酶缺乏症
9.
17α-hydroxylase/17, 20-lyase Deficiency: 1 Case Report and Literature Review;
17α-羟化酶/17，20碳链裂解酶缺乏症1例报告及文献回顾
10.
Prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency
先天性肾上腺皮质增生症21-羟化酶缺陷的产前诊断一例
11.
Congenital Adrenocortical Hyper plasia:A case of 17α-hydroxylase deficiency
先天性肾上腺皮质增生(17α-羟化酶缺乏症1例报告)
12.
sulfite oxidase deficiency
亚硫酸氧化酶缺乏症
13.
A STUDY ON CORRELATION BETWEEN21-HYDROXYLASE GENE DEFECTS ANDCLINICAL TYPES BY USING PCR-ASO TECH-NIQUE
21－羟化酶基因缺陷与先天性肾上腺皮质增生症临床类型相关性的研究
14.
Phenylketonuria is a condition in which phenylalanine to tyrosine conversion is diminished because the enzyme phenylalanine hydroxylaze is deficient.
苯丙酮酸尿症是一种由于苯丙氨酸羟化酶缺乏，苯丙氨酸转变成酪氨酸的过程被削弱的
15.
Functional Characterization of Novel CYP21 Mutations P459H and R483W Detected in Two Chinese Patients with Simple-virilizing Form of Congenital Adrenal Hyperplasia;
21-羟化酶基因新突变P459H和R483W的功能学研究
16.
17,20-desmolase deficiency
１７,２０－碳链酶缺乏症
17.
reductase deficiency
５α－还原酶缺乏症
18.
myophosphorylase deficiency glycogenosis
肌磷酸化酶缺乏性糖原生成