Detection of Leptospira DNA in patients with aseptic meningitis by PCRROMERO, E. C; BILLERBECK, A. E. C; LANDO, V. S et al.Journal of clinical microbiology (Print). 1998, Vol 36, Num 5, pp 1453-1455, issn 0095-1137Article

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

Genetic linkage studies of thyroid peroxidase (TPO) gene in families with TPO deficiencyMANGKLABRUKS, A; BILLERBECK, A.-E. C; DEGROOT, L. J et al.The Journal of clinical endocrinology and metabolism. 1991, Vol 72, Num 2, pp 471-476, issn 0021-972X, 6 p.Article

Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletionABRAO, M. G; LEITE, M. V; CARVALHO, L. R et al.Clinical endocrinology (Oxford. Print). 2006, Vol 65, Num 3, pp 294-300, issn 0300-0664, 7 p.Article

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

A 138-nucleotide deletion in the thyroglobulin ribonucleic acid messenger in a congenital goiter with defective thyroglobulin synthesisTARGOVNIK, H. M; VONO, J; BILLERBECK, A. E. C et al.The Journal of clinical endocrinology and metabolism. 1995, Vol 80, Num 11, pp 3356-3360, issn 0021-972XArticle

Investigations of the ZFY gene in XX true hermaphroditism and Swyer syndromeDAMIANI, D; BILLERBECK, A. E. C; GOLDBERG, A. C. K et al.Human genetics. 1990, Vol 85, Num 1, pp 85-88, issn 0340-6717, 4 p.Article