SARIKEPE, B. Et Al. 2017. Mutation analysis of GJB2 (connexin 26) and GJB6 (connexin 30) genes in patients with congenital non-syndromic hearing loss around Denizli.. 1. international symposium on inner ear therapies , (Marrakush, Morocco).

SARIKEPE, B., TÜMKAYA, F., BAĞCI, G., ARDIÇ, F. N., & SEMERCİ GÜNDÜZ, C. N., (2017). Mutation analysis of GJB2 (connexin 26) and GJB6 (connexin 30) genes in patients with congenital non-syndromic hearing loss around Denizli. . 1. international symposium on inner ear therapies, Marrakush, Morocco

SARIKEPE, BİLGE Et Al. "Mutation analysis of GJB2 (connexin 26) and GJB6 (connexin 30) genes in patients with congenital non-syndromic hearing loss around Denizli.," 1. international symposium on inner ear therapies, Marrakush, Morocco, 2017

SARIKEPE, BİLGE Et Al. "Mutation analysis of GJB2 (connexin 26) and GJB6 (connexin 30) genes in patients with congenital non-syndromic hearing loss around Denizli.." 1. international symposium on inner ear therapies , Marrakush, Morocco, 2017

SARIKEPE, B. Et Al. (2017) . "Mutation analysis of GJB2 (connexin 26) and GJB6 (connexin 30) genes in patients with congenital non-syndromic hearing loss around Denizli.." 1. international symposium on inner ear therapies , Marrakush, Morocco.

@conferencepaper{conferencepaper, author={BİLGE SARIKEPE Et Al. }, title={Mutation analysis of GJB2 (connexin 26) and GJB6 (connexin 30) genes in patients with congenital non-syndromic hearing loss around Denizli.}, congress name={1. international symposium on inner ear therapies}, city={Marrakush}, country={Morocco}, year={2017}}