Genetics of Childhood Hearing Loss-Reference-Cited by-同舟云学术

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Genetics of Childhood Hearing Loss

Published:2021-12 Issue:6 Volume:54 Page:1081-1092
ISSN:0030-6665
Container-title:Otolaryngologic Clinics of North America
language:en
Short-container-title:Otolaryngologic Clinics of North America

Author:

Mitchell Calli Ober,Morton Cynthia Casson

Funder

National Institute on Deafness and Other Communication Disorders

Manchester Biomedical Research Centre

National Institutes of Health

Publisher

Elsevier BV

Subject

General Medicine,Otorhinolaryngology

Reference49 articles.

1. Future directions for screening and treatment in congenital hearing loss;Thorpe;Precision Clin Med,2020

2. Hearing loss–related issues affecting quality of life in preschool children;Lindburg;Otolaryngol Head Neck Surg,2021

3. Childhood hearing loss strategies for prevention and care;Krug,2016

4. A proposal for comprehensive newborn hearing screening to improve identification of deaf and hard-of-hearing children;Shearer;Genet Med,2019

5. Summary of diagnostics among infants not passing hearing screening,2018

Cited by 10 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. Towards Comprehensive Newborn Hearing and Genetic Screening in Russia: Perspectives of Implementation;Journal of Otorhinolaryngology, Hearing and Balance Medicine;2024-05-15

2. Review and research gap identification in genetics causes of syndromic and nonsyndromic hearing loss in Saudi Arabia;Annals of Human Genetics;2024-03-22

3. Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin America;Genes;2024-01-29

4. Deafness DFNB110 associated with a human MAP3K1 recessive variant recapitulates hearing loss of Map3k1 kinase deficient mice;2023-09-06

5. Trajectory of hearing loss in children with unilateral hearing loss;Frontiers in Pediatrics;2023-04-11

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