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PreviewIssue DateTitleAuthor(s)AdvisorType
2016A case of 46,XY DSD due to a novel mutation in the HSD17B3 genePetroli, R.J.; Soardi, F.C.; Mazzola, T.; Michelato, Dd.P.; Vieira Goes, L.C.; Lima do Nascimento, D.L.; Palandi de Mello, M.; Lopes Monlleó, I.-Outro documento
2018Discrete virilization in girls with the classic form of congenital adrenal hyperplasia: the importance of a detailed genital examination at birthChagas, Letícia Santos Silva; Guerra-Junior, Gil; De-Melo, Maricilda Palandi; Lemos-Marini, Sofia Helena Valente-Outro documento
2016Molecular analysis of NR5A1 gene in a cohort of 96 brazilian patients with 46, XY DSD revealed nine novel mutationsCampos Fabbri, H.; Hiort, O.; Guerra Junior, G.; Maciel-Guerra, A.; Ribeiro de Andrade, J.G.; Maia Costa de Queiroz, C.; Lopes Monlleó, I.; Carvalho Castro, J.; Werner, R.; Palandi de Mello, M.-Outro documento
2016A novel CYP21A2 mutation identified a patient with classical 21-hydroxylase deficiencyMichelato, Dd.P.; Petroli, R.J.; Santos, L.Gd.; Monlleó, I.L.; Mello, M.Pd.-Outro documento
2014An eye on sickle cell retinopathyMelo, Mônica Barbosa de-Outro documento
201646,xy partial gonadal dysgenesis caused by an Xp21.2 interstitial duplication that does not encompass the NR0B1 geneSantos, Ana Paula dos; Piveta, Cristiane dos Santos Cruz; Andrade, Juliana Gabriel Ribeiro de; Fabbri, Helena Campos; Lopes, Vera Lúcia Gil da Silva; Guerra Júniorc, Gil; Guerra, Andréa Trevas Maciel; Mello, Maricilda Palandi-Outro documento
2016Molecular analysis of AR, SRD5A2, NR5A1 and HSD17B3 genes in a brazilian 46,XY DSD cohortPetroli, Reginaldo José; Lessa, Victor José Correia; Vieira, Larissa Clara; Calais, Flávia Leme de; Fabbri, Helena Campos; Henriques, Taciane Barbosa; Piveta, Cristiane dos Santos Cruz; Nascimento, Diogo Lucas Lima do; Mello, Maricilda Palandi de; Monlleó, Isabella Lopes-Outro documento
2016Variability in centromere position in chromosomes 2 and 4 of tropical maize linesAguiar-Perecin, M. L. R.; Mondin, M.; Santos-Serejo, J. A.; Bertao, M. R.; Laborda, P.; Pizzaia, D.-Outro documento
2018A paternally inherited NR5A1 mutation in a case of 46,XY partial gonadal dysgenesisMaciel-Guerra, Andrea; Fabbri-Scallet, Helena; Guerra-Junior, Gil; Mello, Maricilda de-Outro documento
2016Mutations at the SF-1 ligand-binding domain can lead to different effects on DNA binding: report of two novel mutationsFabbri, Helena Campos; Werner, Ralf; Guerra Júnior, Gil; Maciel-Guerra, Andrea Trevas; Andrade, Juliana Gabriel Ribeiro de; Hiort, Olaf; Mello, Maricilda Palandi de-Outro documento