Clinical Utility of Next-generation Sequencing in the Aetiological Diagnosis of Sensorineural Hearing Loss in a Childhood Hearing Loss Unit-Reference-Cited by-同舟云学术

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Clinical Utility of Next-generation Sequencing in the Aetiological Diagnosis of Sensorineural Hearing Loss in a Childhood Hearing Loss Unit

Published:2020-05 Issue:3 Volume:71 Page:166-174
ISSN:2173-5735
Container-title:Acta Otorrinolaringologica (English Edition)
language:en
Short-container-title:Acta Otorrinolaringologica (English Edition)

Author:

Costales María,Diñeiro Marta,Cifuentes Guadalupe Á.,Capín Raquel,Otero Andrea,Viejo-Díaz Mónica,Plasencia Ana,Núñez Faustino,Gómez Justo Ramón,Llorente José Luis,Cadiñanos Juan,Cabanillas Rubén

Funder

María Cristina Masaveu Peterson Foundation

Publisher

Elsevier BV

Reference24 articles.

1. Sensorineural hearing loss in children;Smith;Lancet.,2005

2. American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss;Alford;Genet Med.,2014

3. Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing;Shearer;Proc Natl Acad Sci U S A.,2010

4. Hereditary hearing loss: genetic counselling;Cabanillas Farpón;Acta Otorrinolaringol Esp.,2012

5. A next-generation sequencing gene panel (MiamiOtoGenes) for comprehensive analysis of deafness genes;Tekin;Hear Res.,2016

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Prevalence and Characteristics of STRC Gene Mutations (DFNB16): A Systematic Review and Meta-Analysis;Frontiers in Genetics;2021-09-21

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