Browsing by Author Ramos, Priscila Zonzini

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Showing results 1 to 5 of 5
PreviewIssue DateTitleAuthor(s)AdvisorType
2013Optimization Of Simultaneous Screening Of The Main Mutations Involved In Non-syndromic Deafness Using The Taqman® Openarray™ Genotyping Platform.Martins, Fábio Tadeu Arrojo; Ramos, Priscila Zonzini; Svidnicki, Maria Carolina Costa Melo; Castilho, Arthur Menino; Sartorato, Edi Lúcia-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
2013Molecular Analysis Of Slc26a4 Gene In Patients With Nonsyndromic Hearing Loss And Eva: Identification Of Two Novel Mutations In Brazilian Patients.de Moraes, Vanessa Cristine Sousa; dos Santos, Nathalia Zocal Pereira; Ramos, Priscila Zonzini; Svidnicki, Maria Carolina Costa Melo; Castilho, Arthur Menino; Sartorato, Edi Lúcia-Artigo de periódico
2015Screening Of Genetic Alterations Related To Non-syndromic Hearing Loss Using Massarray Iplex® Technology.Svidnicki, Maria Carolina Costa Melo; Silva-Costa, Sueli Matilde; Ramos, Priscila Zonzini; dos Santos, Nathalia Zocal Pereira; Martins, Fábio Tadeu Arrojo; Castilho, Arthur Menino; Sartorato, Edi Lúcia-Artigo de periódico
2016Auditory neuropathy: clinical evaluation and diagnostic approachCarvalho, Guilherme Machado; Leão, Beatriz Prista; Ramos, Priscila Zonzini; Guimarães, Alexandre Caixeta; Castilho, Arthur Menino; Sartorato, Edi Lúcia-Artigo