Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia
Article first published online: 23 APR 2008
© 2008 The Authors Journal compilation © 2008 Blackwell Munksgaard
Volume 73, Issue 6, pages 554–565, June 2008
How to Cite
Tekin, M., Öztürkmen Akay, H., Fitoz, S., Birnbaum, S., Cengiz, F., Sennaroğlu, L., İncesulu, A., Yüksel Konuk, E., Hasanefendioğlu Bayrak, A., Şentürk, S., Cebeci, İ., Ütine, G., Tunçbilek, E., Nance, W. and Duman, D. (2008), Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia. Clinical Genetics, 73: 554–565. doi: 10.1111/j.1399-0004.2008.01004.x
- Issue published online: 7 MAY 2008
- Article first published online: 23 APR 2008
- Received 7 September 2007, revised and accepted for publication 23 January 2008
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