Evaluation of Family History of Permanent Hearing Loss in Childhood as a Risk Indicator in Universal Screening-Reference-Cited by-同舟云学术

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Evaluation of Family History of Permanent Hearing Loss in Childhood as a Risk Indicator in Universal Screening

Published:2017-05 Issue:3 Volume:68 Page:157-163
ISSN:2173-5735
Container-title:Acta Otorrinolaringologica (English Edition)
language:en
Short-container-title:Acta Otorrinolaringologica (English Edition)

Author:

Valido Quintana Mercedes,Oviedo Santos Ángeles,Borkoski Barreiro Silvia,Santana Rodríguez Alfredo,Ramos Macías Ángel

Publisher

Elsevier BV

Reference27 articles.

1. Despistaje de hipoacusia neonatal: resultados después de 3 años de iniciar nuestro programa;Méndez;Acta Otorrinolaringol Esp,2005

2. Control de calidad de un programa de detección, diagnóstico e intervención precoz de la hipoacusia en recién nacidos. Documento oficial de la Comisión para la Detección Precoz de la Hipoacusia;Marco;Acta Otorrinolaringol Esp,2004

3. Connexin-26 mutations in sporadic and inherited sensorineural deafness;Estivill;Lancet,1998

4. High carrier frequency of the 35delG deafness mutation in European populations;Gasparini;Eur J Hum Genet,2000

5. Connexin 26 mutations in hereditary nonsyndromic sensorineural deafness;Kelsell;Nature,1997

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