Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.
Tekin, M.; Akay, H. Öztürkmen; Fitoz, S.; Birnbaum, S.; Cengiz, F. B.; Sennaroğlu, L.; İncesulu, A.; Konuk, E. B. Yüksel; Bayrak, A. Hasanefendioğlu; Şentürk, S.; Cebeci, İ; Ütine, G. E.; Tunçbilek, E.; Nance, W. E.; Duman, D.; Clinical Genetics, 2008, vol. 73, issue 6, p 554, ISSN 00099163. ISBN 13990004.

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