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3. Congenital Middle Ear Malformation with Common Deafness Gene Mutation Analysis: A Review of 813 Profound Sensorineural Hearing Loss Child Patients. Issue 3 (26th December 2019)

7. The role of transcription factors of neurosensory cells in non-syndromic sensorineural hearing loss with or without inner ear malformation. (3rd March 2016)