AYDIN 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 .

AYDIN KÖKER, S., KÖKER, A., NEERMAN-ARBEZ, M., Tuncer, G. O., AKBAŞ, Y., 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.

AYDIN 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, 2020

AYDIN 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, 2020

AYDIN 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.

@article{article, author={Sultan AYDIN 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}