Tekin, M. Et Al. 2008. Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.. Clinical genetics , vol.73, no.6 , 554-65.

Tekin, M., Akay, H. O., Fitoz, S., Birnbaum, S., Cengiz, F. B., Sennaroglu, L., ... Incesulu, A.(2008). Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.. Clinical genetics , vol.73, no.6, 554-65.

Tekin, M. Et Al. "Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.," Clinical genetics , vol.73, no.6, 554-65, 2008

Tekin, M. Et Al. "Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.." Clinical genetics , vol.73, no.6, pp.554-65, 2008

Tekin, M. Et Al. (2008) . "Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.." Clinical genetics , vol.73, no.6, pp.554-65.

@article{article, author={M. Tekin Et Al. }, title={Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.}, journal={Clinical genetics}, year=2008, pages={554-65} }