Browsing by Author de Oliveira, Camila Andréa

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PreviewIssue DateTitleAuthor(s)AdvisorType
2007Molecular Genetics Study Of Deafness In Brazil: 8-year Experience.de Oliveira, Camila Andréa; Alexandrino, Fabiana; Christiani, Thalita Vitachi; Steiner, Carlos Eduardo; Cunha, José Luiz Rosemberis; Guerra, Andréa Trevas Maciel; Sartorato, Edi Lúcia-Artigo de periódico
2009Connexin Mutations In Brazilian Patients With Skin Disorders With Or Without Hearing Loss.Alexandrino, Fabiana; de Oliveira, Camila Andréa; Magalhães, Renata F; Florence, Michelle E B; de Souza, Elemir M; Sartorato, Edi Lúcia-Artigo de periódico
2007Molecular Study In Brazilian Cochlear Implant Recipients.Christiani, Thalita Vitachi; Alexandrino, Fabiana; de Oliveira, Camila Andréa; Amantini, Regina Célia Bortoleto; Bevilacqua, Maria Cecília; Filho, Orozimbo Alves Costa; Porto, Paulo; Sartorato, Edi Lúcia-Artigo de periódico
2015Single Nucleotide Polymorphisms Of The Gjb2 And Gjb6 Genes Are Associated With Autosomal Recessive Nonsyndromic Hearing Loss.Grillo, Ana Paula; de Oliveira, Flávia Marcorin; de Carvalho, Gabriela Queila; Medrano, Ruan Felipe Vieira; da Silva-Costa, Sueli Matilde; Sartorato, Edi Lúcia; de Oliveira, Camila Andréa-Artigo de periódico
Showing results 1 to 4 of 4