Tekin, M. 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. American Journal of Human Genetics , vol.80, no.2 , 338-344.

Tekin, M., Hişmi, B., Fitoz, S., Özdaǧ, H., Cengiz, F. B., Sirmaci, A., ... Aslan, I.(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. American Journal of Human Genetics , vol.80, no.2, 338-344.

Tekin, Mustafa 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," American Journal of Human Genetics , vol.80, no.2, 338-344, 2007

Tekin, Mustafa 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." American Journal of Human Genetics , vol.80, no.2, pp.338-344, 2007

Tekin, M. 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." American Journal of Human Genetics , vol.80, no.2, pp.338-344.

@article{article, author={Mustafa Tekin Et Al. }, title={Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia}, journal={American Journal of Human Genetics}, year=2007, pages={338-344} }