APA引用形式

Cai, R., Li, Y., Wang, W., Gao, X., Liu, M., Diao, Y., . . . Feng, Q. (2018). A novel fibrinogen variant in a Chinese pedigree with congenital dysfibrinogenemia caused by FGA P. Arg38Thr mutation: A case report. Medicine (Baltimore).

シカゴスタイル引用形

Cai, Ruimin, Yi Li, Wenyang Wang, Xue Gao, Meirong Liu, Youxiang Diao, Yi Tang, , Qiang Feng. "A Novel Fibrinogen Variant in a Chinese Pedigree With Congenital Dysfibrinogenemia Caused By FGA P. Arg38Thr Mutation: A Case Report." Medicine (Baltimore) 2018.

MLA引用形式

Cai, Ruimin, et al. "A Novel Fibrinogen Variant in a Chinese Pedigree With Congenital Dysfibrinogenemia Caused By FGA P. Arg38Thr Mutation: A Case Report." Medicine (Baltimore) 2018.