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Clinical Endocrinology|May 3, 2000
Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiencyT A Bachega, A E Billerbeck, J A Marcondes, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|May 1, 2001
Adrenal nodules in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: regression after adequate hormonal controlL R Giacaglia, B B Mendonca, G Madureira, et al.Revista Do Hospital Das Clinicas|August 12, 1998
Protocol for rapid fetal sex determination in chorionic villus through polimerase chain reactionS Domenice, A E Billerbeck, R O Rocha, et al.The Journal of Clinical Endocrinology and Metabolism|December 16, 1998
Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiencyT A Bachega, A E Billerbeck, G Madureira, et al.Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|September 27, 2000
21-Hydroxylase deficiency in BrazilT A Bachega, A E Billerbeck, G Madureira, et al.Human Heredity|April 3, 1999
Low frequency of CYP2B deletions in Brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylas deficiencyT A Bachega, A E Billerbeck, G Madureira, et al.The Journal of Clinical Endocrinology and Metabolism|August 12, 1999
A novel missense mutation, GLY424SER, in Brazilian patients with 21-hydroxylase deficiencyA E Billerbeck, T A Bachega, E T Frazatto, et al.Clinical Genetics|September 18, 2012
The effect of fetal androgen metabolism-related gene variants on external genitalia virilization in congenital adrenal hyperplasiaL C Kaupert, S H V Lemos-Marini, M P De Mello, et al.Pageof 1