Genetic screening as an adjunct to universal newborn hearing screening: literature review and implications for non-congenital pre-lingual hearing loss-Reference-Cited by-同舟云学术

Genetic screening as an adjunct to universal newborn hearing screening: literature review and implications for non-congenital pre-lingual hearing loss

Published:2019-07-02 Issue:12 Volume:58 Page:834-850
ISSN:1499-2027
Container-title:International Journal of Audiology
language:en
Short-container-title:International Journal of Audiology

Author:

D’Aguillo Christine¹,Bressler Sara¹,Yan Denise¹,Mittal Rahul¹^ORCID,Fifer Robert²,Blanton Susan H.¹³⁴,Liu Xuezhong¹²³⁴⁵

Affiliation:

1. Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, FL, USA;

2. Department of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA;

3. Department of Human Genetics, Dr. John T. Macdonald Foundation, Miami, FL, USA;

4. John P Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA;

5. Tsinghua University School of Medicine, Beijing, PR China

Funder

National Institutes of Health/National Institute on Deafness

Publisher

Informa UK Limited

Subject

Speech and Hearing,Linguistics and Language,Language and Linguistics

Link

https://www.tandfonline.com/doi/pdf/10.1080/14992027.2019.1632499

Reference94 articles.

1. Improving hearing loss gene testing: a systematic review of gene evidence toward more efficient next-generation sequencing–based diagnostic testing and interpretation

2. A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families

3. Year 2007 Position Statement: Principles and Guidelines for Early Hearing Detection and Intervention Programs

4. TBC1D24Mutation Causes Autosomal-Dominant Nonsyndromic Hearing Loss

5. HOMER2, a Stereociliary Scaffolding Protein, Is Essential for Normal Hearing in Humans and Mice

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