1.
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)
2.
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
3.
hydroxylase deficiency
１７α－羟化酶缺乏症
4.
21-hydroxylase deficiency
２１－羟化酶缺乏症
5.
Clinical and molecular genetic analysis for a patient with 17 hydroxylase/17,20 lyase deficiency
1例17α-羟化酶/17,20碳链裂解酶缺陷症的临床和分子遗传分析
6.
hydroxysteroid oxidoreductase deficiency
１７β－羟类固醇氧化还原酶缺乏症
7.
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
8.
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
9.
18-oxylase deficiency
１８－氧化酶缺乏症
10.
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
11.
sulfite oxidase deficiency
亚硫酸氧化酶缺乏症
12.
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
13.
17,20-desmolase deficiency
１７,２０－碳链酶缺乏症
14.
reductase deficiency
５α－还原酶缺乏症
15.
myophosphorylase deficiency glycogenosis
肌磷酸化酶缺乏性糖原生成
16.
Studies on the fermentation conditions of C_(11)α-hydroxylation of 16α,17α-epoxy-4-pregnene-3,20-dione by Cunninghamella elegans
雅致小克银汉霉对16α,17α-环氧黄体酮C_(11)α-羟基化的工艺研究
17.
Studies on the Reaction of C_(11)α-Hydroxylation of 16α,17α-Epoxy Progesterone by Rhiz opus Nigricans in the Two-Liquid-Phase System
双液相体系下对黑根霉C_(11)α-羟基化16α,17α-环氧孕酮的研究
18.
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