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Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia

Homozygous MutationsDevelopmental BiologySyndromic Deafness CharacterizedMendelian DisorderGenetic DisorderGeneticsAudiologyInner Ear AgenesisArtsMedicineCell BiologyMicrotiaHearing Loss