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

Internet

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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