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Journal of Clinical Microbiology|May 9, 1998
Detection of Leptospira DNA in patients with aseptic meningitis by PCRE C Romero, A E Billerbeck, V S Lando, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|June 1, 1996
Molecular analysis of sex determination in sex-reversed and true hermaphroditismS B Copelli, C Bergadá, A E Billerbeck, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1991
Genetic linkage studies of thyroid peroxidase (TPO) gene in families with TPO deficiencyA Mangklabruks, A E Billerbeck, B Wajchenberg, et al.
Human Mutation|September 30, 1999
A novel point mutation (R840S) in the androgen receptor in a Brazilian family with partial androgen insensitivity syndromeK F Melo, A C Latronico, E M Costa, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1995
A 138-nucleotide deletion in the thyroglobulin ribonucleic acid messenger in a congenital goiter with defective thyroglobulin synthesisH M Targovnik, J Vono, A E Billerbeck, 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.
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.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|March 21, 2001
Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absence of SRY sequence in gonadal tissueS Domenice, M Y Nishi, A E Billerbeck, 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.
The Journal of Clinical Endocrinology and Metabolism|July 14, 1998
A unique constitutively activating mutation in third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious pubertyA C Latronico, A N Abell, I J Arnhold, et al.
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