Two novel mutations with 17 hydroxylase deficiency – Alpha and beta presenting as 46XY disorders of sexual development. Indian Journal of Child Health, [S. l.], v. 6, n. 11, p. 623–626, 2019. DOI: 10.32677/IJCH.2019.v06.i11.013. Disponível em: https://mansapublishers.com/index.php/ijch/article/view/1875.. Acesso em: 13 apr. 2025.