Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia

MLA

Öztan Yasun, et al. Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia. Feb. 2007. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi.dedup.....befa7e0aeb93575d25e75e787adeef44&authtype=sso&custid=ns315887.

APA

Öztan Yasun, E. Berrin Yüksel-Konuk, Suat Fitoz, Hilal Özdağ, Asli Sirmaci, Nejat Akar, Seda Taşır Yılmaz, Bora İnceoğlu, İdil Aslan, Filiz Basak Cengiz, Mustafa Tekin, & Burcu Ozturk Hismi. (2007). Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia.

Chicago

Öztan Yasun, E. Berrin Yüksel-Konuk, Suat Fitoz, Hilal Özdağ, Asli Sirmaci, Nejat Akar, Seda Taşır Yılmaz, et al. 2007. “Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia,” February. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi.dedup.....befa7e0aeb93575d25e75e787adeef44&authtype=sso&custid=ns315887.