Evirgen, N. Et Al. 2008. Genotyping for Cx26 and Cx30 mutations in cases with congenital hearing loss. GENETIC TESTING , vol.12, no.2 , 253-256.

Evirgen, N., Solak, M., Derekoy, S., Erdogan, M., Yildiz, H., Eser, B., ... Arikan, S.(2008). Genotyping for Cx26 and Cx30 mutations in cases with congenital hearing loss. GENETIC TESTING , vol.12, no.2, 253-256.

Evirgen, Neslihan Et Al. "Genotyping for Cx26 and Cx30 mutations in cases with congenital hearing loss," GENETIC TESTING , vol.12, no.2, 253-256, 2008

Evirgen, Neslihan Et Al. "Genotyping for Cx26 and Cx30 mutations in cases with congenital hearing loss." GENETIC TESTING , vol.12, no.2, pp.253-256, 2008

Evirgen, N. Et Al. (2008) . "Genotyping for Cx26 and Cx30 mutations in cases with congenital hearing loss." GENETIC TESTING , vol.12, no.2, pp.253-256.

@article{article, author={Neslihan Evirgen Et Al. }, title={Genotyping for Cx26 and Cx30 mutations in cases with congenital hearing loss}, journal={GENETIC TESTING}, year=2008, pages={253-256} }