Aydın Köker, S. Et Al. 2020. A Novel Frameshift Mutation in the FGA Gene (c.196 delT) Leading to Congenital Afibrinogenemia.. Journal Of Pediatric Hematology Oncology , vol.42, no.2 , 98-99.

Aydın Köker, S., Köker, A., Neerman-Arbez, M., Öz Tunçer, G., Akbaş, Y., Tural Kara, T., ... Çoban, Y.(2020). A Novel Frameshift Mutation in the FGA Gene (c.196 delT) Leading to Congenital Afibrinogenemia.. Journal Of Pediatric Hematology Oncology , vol.42, no.2, 98-99.

Aydın Köker, Sultan Et Al. "A Novel Frameshift Mutation in the FGA Gene (c.196 delT) Leading to Congenital Afibrinogenemia.," Journal Of Pediatric Hematology Oncology , vol.42, no.2, 98-99, 2020

Aydın Köker, Sultan A. Et Al. "A Novel Frameshift Mutation in the FGA Gene (c.196 delT) Leading to Congenital Afibrinogenemia.." Journal Of Pediatric Hematology Oncology , vol.42, no.2, pp.98-99, 2020

Aydın Köker, S. Et Al. (2020) . "A Novel Frameshift Mutation in the FGA Gene (c.196 delT) Leading to Congenital Afibrinogenemia.." Journal Of Pediatric Hematology Oncology , vol.42, no.2, pp.98-99.

@article{article, author={Sultan Aydın Köker Et Al. }, title={A Novel Frameshift Mutation in the FGA Gene (c.196 delT) Leading to Congenital Afibrinogenemia.}, journal={Journal Of Pediatric Hematology Oncology}, year=2020, pages={98-99} }