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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.Pageof 3