DİNÇER, T. Et Al. 2016. A novel splicing site mutation of PLK4 that is required for centriole biogenesis and genomic stability causes Seckel Syndrome.. The European Human Genetics Conference , (Barselona, Spain), 354.

DİNÇER, T., BUDAK, G., SEMERCİ, C. N., ÖLMEZ, A., DODURGA, Y., ÖZMERT, Ö. M., ... TORAMAN, B.(2016). A novel splicing site mutation of PLK4 that is required for centriole biogenesis and genomic stability causes Seckel Syndrome. . The European Human Genetics Conference (pp.354). Barselona, Spain

DİNÇER, TUBA Et Al. "A novel splicing site mutation of PLK4 that is required for centriole biogenesis and genomic stability causes Seckel Syndrome.," The European Human Genetics Conference, Barselona, Spain, 2016

DİNÇER, TUBA Et Al. "A novel splicing site mutation of PLK4 that is required for centriole biogenesis and genomic stability causes Seckel Syndrome.." The European Human Genetics Conference , Barselona, Spain, pp.354, 2016

DİNÇER, T. Et Al. (2016) . "A novel splicing site mutation of PLK4 that is required for centriole biogenesis and genomic stability causes Seckel Syndrome.." The European Human Genetics Conference , Barselona, Spain, p.354.

@conferencepaper{conferencepaper, author={TUBA DİNÇER Et Al. }, title={A novel splicing site mutation of PLK4 that is required for centriole biogenesis and genomic stability causes Seckel Syndrome.}, congress name={The European Human Genetics Conference}, city={Barselona}, country={Spain}, year={2016}, pages={354} }