Associated Papers
Assisted Reproduction Technology Treatment Outcomes in Female Carriers of 21-Hydroxylase Deficiency.
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The Journal of Clinical Endocrinology and Metabolism, 2025
Congenital Adrenal Hyperplasia (CAH) due to 21-Hydroxylase Deficiency: A Comprehensive Focus on 233 Pathogenic Variants of CYP21A2 Gene.
Concolino P et al.
Molecular Diagnosis & Therapy, 2018
Characterization of novel missense mutations in CYP21 causing congenital adrenal hyperplasia.
Robins T et al.
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