TÜRKYILMAZ, A. Et Al. 2018. FGF3 gene mutations related to two syndromic Congenital deafness cases: Congenital deafness with inner ear agenesis (Michel aplasia), microtia, and microdontia and Otodental dysplasia. 51st European Society of Human Genetics Conference , (Milan, Italy), 893.

TÜRKYILMAZ, A., GEÇKİNLİ, B. B., ARSLAN ATEŞ, E., SÖYLEMEZ, M. A., GÜNEY, A. İ., ATA, P., ... ARMAN, A.(2018). FGF3 gene mutations related to two syndromic Congenital deafness cases: Congenital deafness with inner ear agenesis (Michel aplasia), microtia, and microdontia and Otodental dysplasia . 51st European Society of Human Genetics Conference (pp.893). Milan, Italy

TÜRKYILMAZ, AYBERK Et Al. "FGF3 gene mutations related to two syndromic Congenital deafness cases: Congenital deafness with inner ear agenesis (Michel aplasia), microtia, and microdontia and Otodental dysplasia," 51st European Society of Human Genetics Conference, Milan, Italy, 2018

TÜRKYILMAZ, AYBERK Et Al. "FGF3 gene mutations related to two syndromic Congenital deafness cases: Congenital deafness with inner ear agenesis (Michel aplasia), microtia, and microdontia and Otodental dysplasia." 51st European Society of Human Genetics Conference , Milan, Italy, pp.893, 2018

TÜRKYILMAZ, A. Et Al. (2018) . "FGF3 gene mutations related to two syndromic Congenital deafness cases: Congenital deafness with inner ear agenesis (Michel aplasia), microtia, and microdontia and Otodental dysplasia." 51st European Society of Human Genetics Conference , Milan, Italy, p.893.

@conferencepaper{conferencepaper, author={AYBERK TÜRKYILMAZ Et Al. }, title={FGF3 gene mutations related to two syndromic Congenital deafness cases: Congenital deafness with inner ear agenesis (Michel aplasia), microtia, and microdontia and Otodental dysplasia}, congress name={51st European Society of Human Genetics Conference}, city={Milan}, country={Italy}, year={2018}, pages={893} }