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   Christine D’Aguillo et al, 2019, International Journal of Audiology CrossRef
2. Pregestational screening of hereditary deafness genes carriers in 10,684 normal pregnant women in Zhuzhou, China
   Mingming Qi et al, 2021, Birth Defects Research CrossRef
3. Prevalence of the mitochondrial 1555 A>G and 1494 C>T mutations in a community-dwelling population in Japan
   Yasunori Maeda et al, 2020, Human Genome Variation CrossRef
4. Low frequency of SLC26A4 c.919-2A > G variant among patients with nonsyndromic hearing loss in Yunnan of Southwest China
   Yan-Qiong Li et al, 2024, BMC Medical Genomics CrossRef
5. Investigation of MYO15A and MYO7A Mutations in Iranian Patients with Nonsyndromic Hearing Loss
   Mahsa Farjami et al, 2021, Fetal and Pediatric Pathology CrossRef
6. Genetic testing involving 100 common mutations for antenatal diagnosis of hereditary hearing loss in Chongqing, China
   Hua Hu et al, 2021, Medicine CrossRef