Genomic analysis of inherited hearing loss in the Palestinian population | PNAS
Comprehensive genetic testing of Chinese SNHL patients and variants interpretation using ACMG guidelines and ethnically matched normal controls | European Journal of Human Genetics
Genes | Free Full-Text | Lights and Shadows in the Genetics of Syndromic and Non-Syndromic Hearing Loss in the Italian Population
Molecular diagnose of a large hearing loss population from China by targeted genome sequencing | Journal of Human Genetics
Developed clinically-actionable gene panels for hearing loss and blindness - Rubén Cabanillas Precision Consulting
Hereditary Hearing Loss: Common and Non-Syndromic
Inheritance pattern of identified genes for genetic hearing loss. Drawn... | Download Scientific Diagram
What you need to know about recent advances in genetics of hearing loss in the newborn | ENT & Audiology News
Genetic Sensorineural Hearing Loss | SpringerLink
Exome sequencing utility in defining the genetic landscape of hearing loss and novel‐gene discovery in Iran - Mohseni - 2021 - Clinical Genetics - Wiley Online Library
IJMS | Free Full-Text | Spectrum of Genes for Non-GJB2-Related Non-Syndromic Hearing Loss in the Russian Population Revealed by a Targeted Deafness Gene Panel
Improving hearing loss gene testing: a systematic review of gene evidence toward more efficient next-generation sequencing–based diagnostic testing and interpretation | Genetics in Medicine
Genetic screening of a Chinese cohort of children with hearing loss using a next-generation sequencing panel | Human Genomics | Full Text
Genomic testing for deafness and its implications | ENT & Audiology News
American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss - ScienceDirect
Potential treatments for genetic hearing loss in humans: current conundrums | Gene Therapy
Non-syndromic hearing loss genes and the related mutations detected... | Download Table
Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes | Orphanet Journal of Rare Diseases | Full Text
IJMS | Free Full-Text | Genetic Etiology of Nonsyndromic Hearing Loss in Hungarian Patients
Frontiers | Utility of Whole Genome Sequencing for Population Screening of Deafness-Related Genetic Variants and Cytomegalovirus Infection in Newborns
Frontiers | Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number
Hereditary Hearing Loss: Genetic Counselling | Semantic Scholar
OtoGenome™ Test for Hearing Loss and Related Syndrome (110 Genes) | Partners Personalized Medicine
Non-Syndromic Genetic Deafness disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Nonsyndromic deafness genes discovered via whole-exome sequencing | Download Table
Clinical evaluation and etiologic diagnosis of hearing loss: A clinical practice resource of the American College of Medical Gen
