Cengiz, F. B. Et Al. 2010. Recurrent and private MYO15A mutations are associated with deafness in the Turkish population. Genetic Testing and Molecular Biomarkers , vol.14, no.4 , 543-550.

Cengiz, F. B., Duman, D., Sirmaci, A., Tokgöz-Yilmaz, S., Erbek, S., Öztürkmen-Akay, H., ... Incesulu, A.(2010). Recurrent and private MYO15A mutations are associated with deafness in the Turkish population. Genetic Testing and Molecular Biomarkers , vol.14, no.4, 543-550.

Cengiz, F. Et Al. "Recurrent and private MYO15A mutations are associated with deafness in the Turkish population," Genetic Testing and Molecular Biomarkers , vol.14, no.4, 543-550, 2010

Cengiz, F. B. Et Al. "Recurrent and private MYO15A mutations are associated with deafness in the Turkish population." Genetic Testing and Molecular Biomarkers , vol.14, no.4, pp.543-550, 2010

Cengiz, F. B. Et Al. (2010) . "Recurrent and private MYO15A mutations are associated with deafness in the Turkish population." Genetic Testing and Molecular Biomarkers , vol.14, no.4, pp.543-550.

@article{article, author={F. Basak Cengiz Et Al. }, title={Recurrent and private MYO15A mutations are associated with deafness in the Turkish population}, journal={Genetic Testing and Molecular Biomarkers}, year=2010, pages={543-550} }