ÇETİNKAYA, A. Et Al. 2016. Loss of function mutations in ELMO2 impeding RSC1 signalling and cell migration cause intraosseous vascular malformation. European Society of Human Genetics Conference .

ÇETİNKAYA, A., Xiong, J., VARGEL, İ., KÖSEMEHMETOĞLU, K., CANTER, H. İ., GERDAN, Ö., ... LONGO, N.(2016). Loss of function mutations in ELMO2 impeding RSC1 signalling and cell migration cause intraosseous vascular malformation . European Society of Human Genetics Conference

ÇETİNKAYA, ARDA Et Al. "Loss of function mutations in ELMO2 impeding RSC1 signalling and cell migration cause intraosseous vascular malformation," European Society of Human Genetics Conference, 2016

ÇETİNKAYA, ARDA Et Al. "Loss of function mutations in ELMO2 impeding RSC1 signalling and cell migration cause intraosseous vascular malformation." European Society of Human Genetics Conference , 2016

ÇETİNKAYA, A. Et Al. (2016) . "Loss of function mutations in ELMO2 impeding RSC1 signalling and cell migration cause intraosseous vascular malformation." European Society of Human Genetics Conference .

@conferencepaper{conferencepaper, author={ARDA ÇETİNKAYA Et Al. }, title={Loss of function mutations in ELMO2 impeding RSC1 signalling and cell migration cause intraosseous vascular malformation}, congress name={European Society of Human Genetics Conference}, city={}, country={}, year={2016}}