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




February 2007

Copyright © 2007, Elsevier

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