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European Journal of Endocrinology, ISSN 0804-4643, 04/2017, Volume 176, Issue 4, pp. R167 - R181
Journal Article
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, ISSN 1003-9406, 02/2019, Volume 36, Issue 2, pp. 103 - 107
Journal Article
Journal Article
07/2011
Congenital adrenal hyperplasia (CAH) is characterized by impaired biosynthesis of cortisol. 21-hydroxylase deficiency is the most common cause of CAH affecting... 
21 Hydroxylase Deficiency | Molecular Genetics | Congenital Adrenal Hyperplasia | Iranian population
Web Resource
Middle East Fertility Society Journal, ISSN 1110-5690, 06/2014, Volume 19, Issue 2, pp. 89 - 95
To investigate fertility in a sample of Tunisian patients with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. Tunisian bicentric... 
Testicular adrenal rest tumours | Hyperandrogenism | 21 Hydroxylase deficiency | Congenital adrenal hyperplasia | Fertility
Journal Article
MEDECINE NUCLEAIRE-IMAGERIE FONCTIONNELLE ET METABOLIQUE, ISSN 0928-1258, 01/2013, Volume 37, Issue 1, pp. 4 - 7
A unit taking care of adults with congenital 21 hydroxylase deficiency (CAH) includes patients with classic CAH, comprising the salt-wasting and the... 
WOMEN | Genetic counseling | Male fertility | Female fertility | CONGENITAL ADRENAL-HYPERPLASIA | RISK | 21 hydroxylase deficiency | PATHOLOGY | FERTILITY
Journal Article
Journal Article
Annals of Pediatric Endocrinology & Metabolism, ISSN 2287-1012, 09/2013, Volume 18, Issue 3, pp. 128 - 134
The purpose of the study was to evaluate endocrine patterns of patients with congenital adrenal hyperplasia and each gene mutation and to analyze the... 
Phenotype | 21 hydroxylase deficiency | Human CYP21A2 protein | genotype | Genotype | Original
Journal Article