Pages that link to "Q34779797"
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The following pages link to Prevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern China. (Q34779797):
Displaying 6 items.
- Characterization of ATPase Activity of P2RX2 Cation Channel (Q27307804) (← links)
- Genetic frequencies related to severe or profound sensorineural hearing loss in Inner Mongolia Autonomous Region (Q30368252) (← links)
- Navigating genetic diagnostics in patients with hearing loss. (Q38934723) (← links)
- Recent Advancements in the Regeneration of Auditory Hair Cells and Hearing Restoration (Q41170353) (← links)
- Mutation analysis of common deafness genes among 1,201 patients with non-syndromic hearing loss in Shanxi Province (Q64264945) (← links)
- Three years of follow-up of otodental syndrome in 3-year-old Chinese boy: a rare case report (Q92180323) (← links)