1.
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
2.
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
3.
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
4.
hydroxylase deficiency
１７α－羟化酶缺乏症
5.
21-hydroxylase deficiency
２１－羟化酶缺乏症
6.
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
7.
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
8.
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
9.
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
10.
hydroxysteroid oxidoreductase deficiency
１７β－羟类固醇氧化还原酶缺乏症
11.
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
12.
Laboratory diagnosis of leukocyte myeloperoxidase deficiency
白细胞髓过氧化物酶缺陷症的实验诊断
13.
18-oxylase deficiency
１８－氧化酶缺乏症
14.
Association between Attention Deficit Hyperactivity Disorder and Single Nucleotide Polymorphisms of Tryptophan Hydroxylase 2 Gene
注意缺陷多动障碍与色氨酸羟化酶2基因多态性的关系
15.
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)
16.
sulfite oxidase deficiency
亚硫酸氧化酶缺乏症
17.
The Correlation between Dopamine Beta Hydroxylase Gene、ABO Blood Type Gene Polymorphism and Attention Deficit Hyperactivity Disorder;
注意缺陷多动障碍与多巴胺β羟化酶基因及ABO血型基因的关联分析
18.
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