KALAY, E. 2006. Mutations in GJB2, TMC1, TMPRSS3 and MYO15A cause autosomal recessive nonsyndromic hearing loss in Turkish patients.. European Human Genetics Conference , (Amsterdam, Netherlands), 141.

KALAY, E., (2006). Mutations in GJB2, TMC1, TMPRSS3 and MYO15A cause autosomal recessive nonsyndromic hearing loss in Turkish patients. . European Human Genetics Conference (pp.141). Amsterdam, Netherlands

KALAY, ERSAN. "Mutations in GJB2, TMC1, TMPRSS3 and MYO15A cause autosomal recessive nonsyndromic hearing loss in Turkish patients.," European Human Genetics Conference, Amsterdam, Netherlands, 2006

KALAY, ERSAN. "Mutations in GJB2, TMC1, TMPRSS3 and MYO15A cause autosomal recessive nonsyndromic hearing loss in Turkish patients.." European Human Genetics Conference , Amsterdam, Netherlands, pp.141, 2006

KALAY, E. (2006) . "Mutations in GJB2, TMC1, TMPRSS3 and MYO15A cause autosomal recessive nonsyndromic hearing loss in Turkish patients.." European Human Genetics Conference , Amsterdam, Netherlands, p.141.

@conferencepaper{conferencepaper, author={ERSAN KALAY}, title={Mutations in GJB2, TMC1, TMPRSS3 and MYO15A cause autosomal recessive nonsyndromic hearing loss in Turkish patients.}, congress name={European Human Genetics Conference}, city={Amsterdam}, country={Netherlands}, year={2006}, pages={141} }