Lv4
576 积分 2022-05-29 加入
An interactive human PROS1 variants database provides novel insights into the genetics and phenotypes of inherited protein S deficiency
13天前
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Clinical, Laboratory, and Molecular Aspects of Congenital Fibrinogen Disorders
1个月前
已完结
Essential Thrombocythemia: A Review
11个月前
已完结
Genotype versus laboratory phenotype correlation of defects in natural anticoagulants in patients with venous thromboembolism
1年前
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