Yıldız, K. Ş. Et Al. 2017. Studying the association between sudden hearing loss and DNA N-methyltransferase 1 (DNMT1) genetic polymorphism. Journal of International Advanced Otology , vol.13, no.3 , 313-317.

Yıldız, K. Ş., Durmuş, K., Dönmez, G., Arslan, S., & ALTUNTAŞ, E. E., (2017). Studying the association between sudden hearing loss and DNA N-methyltransferase 1 (DNMT1) genetic polymorphism. Journal of International Advanced Otology , vol.13, no.3, 313-317.

Yıldız, Kübra Et Al. "Studying the association between sudden hearing loss and DNA N-methyltransferase 1 (DNMT1) genetic polymorphism," Journal of International Advanced Otology , vol.13, no.3, 313-317, 2017

Yıldız, Kübra Ş. Et Al. "Studying the association between sudden hearing loss and DNA N-methyltransferase 1 (DNMT1) genetic polymorphism." Journal of International Advanced Otology , vol.13, no.3, pp.313-317, 2017

Yıldız, K. Ş. Et Al. (2017) . "Studying the association between sudden hearing loss and DNA N-methyltransferase 1 (DNMT1) genetic polymorphism." Journal of International Advanced Otology , vol.13, no.3, pp.313-317.

@article{article, author={Kübra Şeker Yıldız Et Al. }, title={Studying the association between sudden hearing loss and DNA N-methyltransferase 1 (DNMT1) genetic polymorphism}, journal={Journal of International Advanced Otology}, year=2017, pages={313-317} }