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Diagnosis routine and approach in genetic sensorineural hearing loss

Aim: To develop a screening in order to determine the more common syndromic and non-syndromic genetic SNHL, considering epidemiological data, information and the development of new technologies; clinical implications and bioethical issues. Materials and Methods: We reviewed the literature in order t...

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Detalles Bibliográficos
Autores principales:	Alves, Fatima Regina Abreu, de Andrade Quintanilha Ribeiro, Fernando
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2015
Materias:	Review Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9445739/ https://www.ncbi.nlm.nih.gov/pubmed/17684664 http://dx.doi.org/10.1016/S1808-8694(15)30087-2

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