1. Genetic etiology of non-syndromic hearing loss in Europe
   Ignacio del Castillo et al, 2022, Human Genetics CrossRef
2. WHEN SHOULD ONE LOOK FOR IVS1+1G>A SPLICE MUTATION IN PATIENTS WITH NONSYNDROMIC SENSORINEURAL HEARING LOSS?
   Olga Shubina-Oleinik et al, 2014, Journal of Hearing Science CrossRef
3. Analyses of del(GJB6‐D13S1830) and del(GJB6‐D13S1834) deletions in a large cohort with hearing loss: Caveats to interpretation of molecular test results in multiplex families
   Arti Pandya et al, 2020, Molecular Genetics & Genomic Medicine CrossRef