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Showing results 1 to 13 of 13
PreviewIssue DateTitleAuthor(s)AdvisorType
2008Inhibition Of Cyp21a2 Enzyme Activity Caused By Novel Missense Mutations Identified In Brazilian And Scandinavian Patients.Soardi, F C; Barbaro, M; Lau, I F; Lemos-Marini, S H V; Baptista, M T M; Guerra-Junior, G; Wedell, A; Lajic, S; de Mello, M P-Artigo de periódico
2013New Mutation In The Myocilin Gene Segregates With Juvenile-onset Open-angle Glaucoma In A Brazilian Family.Braghini, Carolina Ayumi; Neshich, Izabella Agostinho Pena; Neshich, Goran; Soardi, Fernanda Caroline; de Mello, Maricilda Palandi; Costa, Vital Paulino; de Vasconcellos, José Paulo Cabral; de Melo, Mônica Barbosa-Artigo de periódico
2000Alpha-globin Genes: Thalassemic And Structural Alterations In A Brazilian Population.Wenning, M R; Kimura, E M; Costa, F F; Saad, S T; Gervásio, S; de Jorge, S B; Borges, E; Silva, N M; Sonati, M F-Artigo de periódico
2008Molecular Genetic Testing Of Hemostasis And Thrombosis In Developing Countries: Achievements, Hopes, And Challenges.Ozelo, Margareth Castro; Zapata Esp, Roman; Qadura, Mohammad; Chegeni, Rouzbeh; Othman, Maha-Artigo de periódico
2014Genetic Predictors Of Long-term Response To Growth Hormone (gh) Therapy In Children With Gh Deficiency And Turner Syndrome: The Influence Of A Socs2 Polymorphism.Braz, Adriana F; Costalonga, Everlayny F; Trarbach, Ericka B; Scalco, Renata C; Malaquias, Alexsandra C; Guerra-Junior, Gil; Antonini, Sonir R R; Mendonca, Berenice B; Arnhold, Ivo J P; Jorge, Alexander A L-Artigo de periódico
2006Spinocerebellar Ataxia Types 2 And 3 Segregating Simultaneously In A Single Family.França, Marcondes C; Calcagnotto, Maria E; da Costa, Jaderson C; Lopes-Cendes, Iscia-Artigo de periódico
2004Structural Alterations Of The Gamma-globin Genes In A Brazilian Population.Duarte, Denise Faustino; Kimura, Elza Myiuki; Albuquerque, Dulcinéia Martins; Pinheiro, Vitória Régia Pereira; Costa, Fernando Ferreira; de Fátima Sonati, Maria-Artigo de periódico
2004Hb Osu-christiansborg [beta52(d3)asp --> Asn]: A De Novo Mutation In Brazil.Rodrigues de Souza, Laudicéia; Kimura, Elza Miyuki; Albuquerque, Dulcinéia Martins; Costa, Fernando Ferreira; de Fátima Sonati, Maria-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
2006Molecular Screening Of Cftr Gene In Brazilian Men With Bilateral Agenesis Of The Vas Deferens.Bertuzzo, Carmen Sílvia; Pinto, Walter-Artigo de periódico
2013Etiologic And Diagnostic Evaluation: Algorithm For Severe To Profound Sensorineural Hearing Loss In Brazil.Ramos, Priscila Zonzini; de Moraes, Vanessa Cristine Sousa; Svidnicki, Maria Carolina Costa Melo; Soki, Marcelo Naoki; Castilho, Arthur Menino; Sartorato, Edi Lúcia-Artigo de periódico
2011Fetal Rhd Genotyping By Analysis Of Maternal Plasma In A Mixed Population.Amaral, Daphne R T; Credidio, Débora C; Pellegrino, Jordão; Castilho, Lilian-Artigo de periódico
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