APA সাইটেশন

Qiao, Y., Zhang, Q., Xu, P., & Deng, Y. (2020). A family study of congenital dysfibrinogenemia caused by a novel mutation in the FGA gene: A case report. Open Med (Wars).

শিকাগো স্টাইলে সাইটেশন

Qiao, Yingli, Qisi Zhang, Poshi Xu, এবং Yuhui Deng. "A Family Study of Congenital Dysfibrinogenemia Caused By a Novel Mutation in the FGA Gene: A Case Report." Open Med (Wars) 2020.

এমএলএ সাইটেশন

Qiao, Yingli, Qisi Zhang, Poshi Xu, এবং Yuhui Deng. "A Family Study of Congenital Dysfibrinogenemia Caused By a Novel Mutation in the FGA Gene: A Case Report." Open Med (Wars) 2020.