Genotype of proband and thrombophilia screening

Blood

Volumn 122, Issue 15, 2013, Pages 2528-2529

  Sandset, Morten ^a  

^a OSLO UNIVERSITY HOSPITAL   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 5 LEIDEN; PROTEIN C; PROTHROMBIN;

BLOOD CLOTTING; CARDIOVASCULAR RISK; GENE INACTIVATION; GENETIC POLYMORPHISM; GENETIC SCREENING; GENOTYPE; HUMAN; PRIORITY JOURNAL; SCREENING; SHORT SURVEY; THROMBOPHILIA; VEIN THROMBOSIS;

EID: 84888254904     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2013-08-519801     Document Type: Short Survey

References (8)

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2. Bertina RM, Koeleman BP, Koster T, et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature. 1994;369(6475):64-67.
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6. Segal JB, Brotman DJ, Necochea AJ, et al. Predictive value of factor V Leiden and prothrombin G20210A in adults with venous thromboembolism and in family members of those with a mutation: a systematic review. JAMA. 2009;301(23):2472-2485.
7. Martinelli I, Bucciarelli P, Margaglione M, De Stefano V, Castaman G, Mannucci PM. The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or both. Br J Haematol. 2000;111(4):1223-1229.
8. Rossi E, Ciminello A, Za T, Betti S, Leone G, De Stefano V. In families with inherited thrombophilia the risk of venous thromboembolism is dependent on the clinical phenotype of the proband. Thromb Haemost. 2011;106(4):646-654.