KANJEE, M. Et Al. 2022. Novel finding in a patient with 17p13.1 deletion syndrome: a case report. European Human Genetics Confrerence 2022 , (Viyana, Austria).

KANJEE, M., CİNKARA, N., YÜCE KAHRAMAN, Ç., & TATAR, A., (2022). Novel finding in a patient with 17p13.1 deletion syndrome: a case report . European Human Genetics Confrerence 2022, Viyana, Austria

KANJEE, MOMEN Et Al. "Novel finding in a patient with 17p13.1 deletion syndrome: a case report," European Human Genetics Confrerence 2022, Viyana, Austria, 2022

KANJEE, MOMEN Et Al. "Novel finding in a patient with 17p13.1 deletion syndrome: a case report." European Human Genetics Confrerence 2022 , Viyana, Austria, 2022

KANJEE, M. Et Al. (2022) . "Novel finding in a patient with 17p13.1 deletion syndrome: a case report." European Human Genetics Confrerence 2022 , Viyana, Austria.

@conferencepaper{conferencepaper, author={MOMEN KANJEE Et Al. }, title={Novel finding in a patient with 17p13.1 deletion syndrome: a case report}, congress name={European Human Genetics Confrerence 2022}, city={Viyana}, country={Austria}, year={2022}}