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.
hydroxylase deficiency
１７α－羟化酶缺乏症
3.
21-hydroxylase deficiency
２１－羟化酶缺乏症
4.
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
5.
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
6.
hydroxysteroid oxidoreductase deficiency
１７β－羟类固醇氧化还原酶缺乏症
7.
18-oxylase deficiency
１８－氧化酶缺乏症
8.
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
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.
sulfite oxidase deficiency
亚硫酸氧化酶缺乏症
11.
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
12.
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)
13.
17,20-desmolase deficiency
１７,２０－碳链酶缺乏症
14.
reductase deficiency
５α－还原酶缺乏症
15.
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
16.
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
17.
congenital aprothrombinemia
先天性凝血酶原缺乏症
18.
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