Molecular diagnose of a large hearing loss population from China by targeted genome sequencing | Journal of Human Genetics
Genetic Sensorineural Hearing Loss | SpringerLink
Diagnosis, Intervention, and Prevention of Genetic Hearing Loss | SpringerLink
Spectrum and frequencies of non GJB2 gene mutations in Czech patients with early non‐syndromic hearing loss detected by gene panel NGS and whole‐exome sequencing - Safka Brozkova - 2020 - Clinical Genetics -
Expert interpretation of genes and variants in hereditary hearing loss
Genetic Testing for Hereditary Hearing Loss
Comprehensive genetic testing improves the clinical diagnosis and medical management of pediatric patients with isolated hearing loss | BMC Medical Genomics | Full Text
Advances in gene therapy hold promise for treating hereditary hearing loss - ScienceDirect
What you need to know about recent advances in genetics of hearing loss in the newborn | ENT & Audiology News
Genetic screening of a Chinese cohort of children with hearing loss using a next-generation sequencing panel | Human Genomics | Full Text
Clinical evaluation and etiologic diagnosis of hearing loss: A clinical practice resource of the American College of Medical Gen
What you need to know about recent advances in genetics of hearing loss in the newborn | ENT & Audiology News
Comprehensive genetic testing of Chinese SNHL patients and variants interpretation using ACMG guidelines and ethnically matched normal controls | European Journal of Human Genetics
Non-syndromic hearing loss gene identification: A brief history and glimpse into the future - ScienceDirect
Mutation screening in non-syndromic hearing loss patients with cochlear implantation by massive parallel sequencing in Taiwan | PLOS ONE
American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss - ScienceDirect
Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss | Scientific Reports
Diagnosing and Preventing Hearing Loss in the Genomic Age - John H. McDermott, Leslie P Molina-Ramírez, Iain A Bruce, Ajit Mahaveer, Mark Turner, Gino Miele, Richard Body, Rachel Mahood, Fiona Ulph, Rhona
Paula Buonfiglio and Dr. Viviana Dalamón have been included in the Hearing Loss Variant Curation Expert Panel. – INGEBI – CONICET
Understanding and treating paediatric hearing impairment - eBioMedicine
Genomic analysis of inherited hearing loss in the Palestinian population | PNAS
Genes | Free Full-Text | Improving the Management of Patients with Hearing Loss by the Implementation of an NGS Panel in Clinical Practice
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
Frontiers | Genetic and Non-genetic Workup for Pediatric Congenital Hearing Loss
About Genetic Testing | A Parent's Guide to Genetics and Hearing Loss | CDC
