au.\*:("BACHEGA, T. A. S. S")
Results 1 to 2 of 2
Selection :
A novel missense mutation, GLY424SER, in Brazilian patients with 21-hydroxylase deficiencyBILLERBECK, A. E. C; BACHEGA, T. A. S. S; FRAZZATTO, E. T et al.The Journal of clinical endocrinology and metabolism. 1999, Vol 84, Num 8, pp 2870-2872, issn 0021-972XArticle
Low frequency of CYP21B deletions in Brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyBACHEGA, T. A. S. S; BILLERBECK, A. E. C; MADUREIRA, G et al.Human heredity. 1999, Vol 49, Num 1, pp 9-14, issn 0001-5652Article
