Associated Papers
Genotypic spectrum of 21-hydroxylase deficiency in an endogamous population.
Mahmoud RAA et al.
Journal of Endocrinological Investigation, 2022
Ehlers-Danlos Syndrome: Molecular and Clinical Characterization of TNXA/TNXB Chimeras in Congenital Adrenal Hyperplasia.
Marino R et al.
The Journal of Clinical Endocrinology and Metabolism, 2021
Mutation analysis of the CYP21A2 gene in the Iranian population.
Rabbani B et al.
Genetic Testing and Molecular Biomarkers, 2012
Molecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene.
Rabbani B et al.
Iranian Journal of Pediatrics, 2011
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