Genetic Information and Precision Medicine in Hearing Loss
Author:
Publisher
Korean Society of Otorhinolaryngology-Head and Neck Surgery
Subject
Otorhinolaryngology,Surgery
Link
http://e-ceo.org/upload/pdf/ceo-2020-01606.pdf
Reference18 articles.
1. Newborn Hearing Screening — A Silent Revolution
2. Sensorineural hearing loss in children
3. Whole-exome sequencing reveals diverse modes of inheritance in sporadic mild to moderate sensorineural hearing loss in a pediatric population
4. Significant Mendelian genetic contribution to pediatric mild-to-moderate hearing loss and its comprehensive diagnostic approach
5. Two Compound Heterozygous Were Identified in SLC26A4 Gene in Two Chinese Families With Enlarged Vestibular Aqueduct
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2. Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin America;Genes;2024-01-29
3. Audiogram Configuration, Molecular Etiology, and Outcome of Cochlear Implantation in Postlingual Auditory Neuropathy Spectrum Disorder;Otology & Neurotology;2023-06-06
4. Improving genetic diagnosis by disease-specific, ACMG/AMP variant interpretation guidelines for hearing loss;Scientific Reports;2022-07-21
5. Molecular aetiology of ski-slope hearing loss and audiological course of cochlear implantees;European Archives of Oto-Rhino-Laryngology;2022-02-25
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