DİNÇER, T. Et Al. 2016. A novel Splicing site mutation of PLK4 that is required for centriole biogenesis and genomiz stability causes SeckelSyndrome. European Society of Human Genetics Congress .

DİNÇER, T., BUDAK YORGANCIOĞLU, G., SEMERCİ, C. N., AKGÜN, Ö., DODURGA, Y., ÖZDEMİR, M. Ö., ... TOROMAN, B.(2016). A novel Splicing site mutation of PLK4 that is required for centriole biogenesis and genomiz stability causes SeckelSyndrome . European Society of Human Genetics Congress

DİNÇER, TUBA Et Al. "A novel Splicing site mutation of PLK4 that is required for centriole biogenesis and genomiz stability causes SeckelSyndrome," European Society of Human Genetics Congress, 2016

DİNÇER, TUBA Et Al. "A novel Splicing site mutation of PLK4 that is required for centriole biogenesis and genomiz stability causes SeckelSyndrome." European Society of Human Genetics Congress , 2016

DİNÇER, T. Et Al. (2016) . "A novel Splicing site mutation of PLK4 that is required for centriole biogenesis and genomiz stability causes SeckelSyndrome." European Society of Human Genetics Congress .

@conferencepaper{conferencepaper, author={TUBA DİNÇER Et Al. }, title={A novel Splicing site mutation of PLK4 that is required for centriole biogenesis and genomiz stability causes SeckelSyndrome}, congress name={European Society of Human Genetics Congress}, city={}, country={}, year={2016}}