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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|August 1, 1995
A novel mutation of the luteinizing hormone receptor gene causing male gonadotropin-independent precocious pubertyA C Latronico, J Anasti, I J Arnhold, et al.Medicine|March 1, 1996
Male pseudohermaphroditism due to steroid 5alpha-reductase 2 deficiency. Diagnosis, psychological evaluation, and managementB B Mendonca, M Inacio, E M Costa, et al.Archives of Disease in Childhood|May 18, 1999
Treatment of gonadotropin dependent precocious puberty due to hypothalamic hamartoma with gonadotropin releasing hormone agonist depotV N de Brito, A C Latronico, I J Arnhold, et al.Journal of Molecular Endocrinology|February 5, 2000
Phenotypic variability and origins of mutations in the gene encoding 3beta-hydroxysteroid dehydrogenase type IIS McCartin, A J Russell, R A Fisher, et al.Journal of Molecular Endocrinology|February 1, 1994
Mutation in 3 beta-hydroxysteroid dehydrogenase type II associated with pseudohermaphroditism in males and premature pubarche or cryptic expression in femalesB B Mendonça, A J Russell, M Vasconcelos-Leite, et al.Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|August 12, 1998
Clinical and molecular characterization of Brazilian patients with growth hormone gene deletionsI J Arnhold, M G Osorio, S B Oliveira, et al.The Journal of Clinical Endocrinology and Metabolism|March 17, 2000
Origin of an ovarian steroid cell tumor causing isosexual pseudoprecocious puberty demonstrated by the expression of adrenal steroidogenic enzymes and adrenocorticotropin receptorC J Lin, A A Jorge, A C Latronico, et al.The Journal of Clinical Endocrinology and Metabolism|September 24, 1998
The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiencyJ D Cogan, W Wu, J A Phillips, et al.Pageof 5