Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.
Tekin M; Oztürkmen Akay H; Fitoz S; Birnbaum S; Cengiz FB; Sennaroğlu L; Incesulu A; Yüksel Konuk EB; Hasanefendioğlu Bayrak A; Sentürk S; Cebeci I; Utine GE; Tunçbilek E; Nance WE; Duman D; Clinical Genetics, 2008, vol. 73, issue 6, p 554, ISSN 13990004. ISBN 13990004.

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