Akcan, M. B. Et Al. 2021. A rare Koolen de Vries syndrome caused by 17q21.31 deletion that encompassing KANSL1 gene. 13th European Cytogenomics Conferece , (Bari, Italy), 0-1.

Akcan, M. B., Kaya, D., Sönmez, V., Kablan, A., Özdemir, Ö., & Sılan, F., (2021). A rare Koolen de Vries syndrome caused by 17q21.31 deletion that encompassing KANSL1 gene . 13th European Cytogenomics Conferece (pp.0-1). Bari, Italy

Akcan, Mehmet Et Al. "A rare Koolen de Vries syndrome caused by 17q21.31 deletion that encompassing KANSL1 gene," 13th European Cytogenomics Conferece, Bari, Italy, 2021

Akcan, Mehmet B. Et Al. "A rare Koolen de Vries syndrome caused by 17q21.31 deletion that encompassing KANSL1 gene." 13th European Cytogenomics Conferece , Bari, Italy, pp.0-1, 2021

Akcan, M. B. Et Al. (2021) . "A rare Koolen de Vries syndrome caused by 17q21.31 deletion that encompassing KANSL1 gene." 13th European Cytogenomics Conferece , Bari, Italy, pp.0-1.

@conferencepaper{conferencepaper, author={Mehmet Berkay Akcan Et Al. }, title={A rare Koolen de Vries syndrome caused by 17q21.31 deletion that encompassing KANSL1 gene}, congress name={13th European Cytogenomics Conferece}, city={Bari}, country={Italy}, year={2021}, pages={0-1} }