Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic...

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 338-344 (February 2007)

DOI: 10.1086/510920

Copyright © 2006 The American Society of Human Genetics Terms and Conditions

http://www.elsevier.com/termsandconditions

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The American Journal of Human Genetics 2007 80, 338-344DOI: (10.1086/510920) Copyright © 2006 The American Society of Human Genetics Terms and Conditions


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Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic...

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