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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 Mustafa Tekin, Burcu Öztürk Hişmi, Suat Fitoz, Hilal Özdağ, Filiz Başak Cengiz, Aslı Sırmacı, İdil Aslan, Bora İnceoğlu, E. Berrin Yüksel- Konuk, Seda Taşır Yılmaz, Öztan Yasun, Nejat Akar The American Journal of Human Genetics Volume 80, Issue 2, Pages (February 2007) DOI: / Copyright © 2006 The American Society of Human Genetics Terms and Conditions Terms and Conditions
Figure 1. The American Journal of Human Genetics , DOI: ( /510920) Copyright © 2006 The American Society of Human Genetics Terms and Conditions Terms and Conditions
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Figure 3. The American Journal of Human Genetics , DOI: ( /510920) Copyright © 2006 The American Society of Human Genetics Terms and Conditions Terms and Conditions
Figure 4. The American Journal of Human Genetics , DOI: ( /510920) Copyright © 2006 The American Society of Human Genetics Terms and Conditions Terms and Conditions
Figure 5. The American Journal of Human Genetics , DOI: ( /510920) Copyright © 2006 The American Society of Human Genetics Terms and Conditions Terms and Conditions
Figure 6. The American Journal of Human Genetics , DOI: ( /510920) Copyright © 2006 The American Society of Human Genetics Terms and Conditions Terms and Conditions
Figure 7. The American Journal of Human Genetics , DOI: ( /510920) Copyright © 2006 The American Society of Human Genetics Terms and Conditions Terms and Conditions
Figure 8. The American Journal of Human Genetics , DOI: ( /510920) Copyright © 2006 The American Society of Human Genetics Terms and Conditions Terms and Conditions
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