Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.Published in:Clinical Genetics, 2008, v. 73, n. 6, p. 554, doi. 10.1111/j.1399-0004.2008.01004.xBy: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.Publication type:Article