• An Asian case of combined 17α-hydroxylase/17,20-lyase deficiency due to homozygous p.R96Q mutation: A case report and review of the literature
• Consequences of steroid-5α-reductase deficiency and inhibition in vertebrates
• Diagnosis and management of patients with sex differentiation disorders: experience at the Unit of Medical Genetics of the University of Zulia, Maracaibo, Venezuela
• Diagnostic interest of Barr chromatin test in sex determination: about one case of male pseudohermaphrodism
• Estrogen: consequences and implications of human mutations in synthesis and action
• Feminizing testicular syndrome with multiple hamartomas and bilateral paratesticular leiomyomas
• Increased 3beta-hydroxysteroid dehydrogenase 2 and 17alpha-hydroxylase activities in a virilized adolescent female with adrenal adenoma: A case report
• Increased 3β-hydroxysteroid dehydrogenase 2 and 17α-hydroxylase activities in a virilized adolescent female with adrenal adenoma: A case report
• Issues inherent to the management of disorders of sex development in Point G Hospital
• Nevus lipomatosus cutaneous superficialis of the clitoris
• Non-human Papillomavirus Cervical Mucinous Adenocarcinoma in a Phenotypic Male with Congenital Adrenal Hyperplasia
• Phenotype-genotype correlation in mutations of the gonadotrophin receptor gene in women
• Reverse (posterior) cloaca with congenital rectal stenosis and pseudohermaphrodism: a rare entity with rare association
• Testosterone metabolism in the estuarine mysid Neomysis integer (Crustacea; Mysidacea) following tributyltin exposure
• The IVS1-2A>G mutation in the SRD5A2 gene predominates in Cypriot patients with 5α reductase deficiency
• WT1 gene mutations in three girls with nephrotic syndrome