Evirgen, N. Et Al. 2007. Genotyping for cx26 and cx30 Gene Mutations in the Cases with Congenital Hearing Loss. II. Congress of Molecular Medicine From Cell to Bedside , (İstanbul, Turkey), 289.

Evirgen, N., Solak, M., Dereköy, S., Erdoğan, M., Eser, B., Yıldız, H., ... ERKOÇ HUT, A.(2007). Genotyping for cx26 and cx30 Gene Mutations in the Cases with Congenital Hearing Loss . II. Congress of Molecular Medicine From Cell to Bedside (pp.289). İstanbul, Turkey

Evirgen, Neslihan Et Al. "Genotyping for cx26 and cx30 Gene Mutations in the Cases with Congenital Hearing Loss," II. Congress of Molecular Medicine From Cell to Bedside, İstanbul, Turkey, 2007

Evirgen, Neslihan Et Al. "Genotyping for cx26 and cx30 Gene Mutations in the Cases with Congenital Hearing Loss." II. Congress of Molecular Medicine From Cell to Bedside , İstanbul, Turkey, pp.289, 2007

Evirgen, N. Et Al. (2007) . "Genotyping for cx26 and cx30 Gene Mutations in the Cases with Congenital Hearing Loss." II. Congress of Molecular Medicine From Cell to Bedside , İstanbul, Turkey, p.289.

@conferencepaper{conferencepaper, author={Neslihan Evirgen Et Al. }, title={Genotyping for cx26 and cx30 Gene Mutations in the Cases with Congenital Hearing Loss}, congress name={II. Congress of Molecular Medicine From Cell to Bedside}, city={İstanbul}, country={Turkey}, year={2007}, pages={289} }