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565 related items for PubMed ID: 17107352

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  • 5. Polymorphisms in the protein C gene as risk factor for venous thrombosis.
    Pomp ER, Doggen CJ, Vos HL, Reitsma PH, Rosendaal FR.
    Thromb Haemost; 2009 Jan; 101(1):62-7. PubMed ID: 19132190
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  • 6. Major and potential prothrombotic genotypes in patients with venous thrombosis and in healthy subjects from Slovenia.
    Bedencic M, Bozic M, Peternel P, Stegnar M.
    Pathophysiol Haemost Thromb; 2008 Jan; 36(2):58-63. PubMed ID: 19127083
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  • 8. The frequency of factor V Leiden and concomitance of factor V Leiden with prothrombin G20210A mutation and methylene tetrahydrofolate reductase C677T gene mutation in healthy population of Denizli, Aegean region of Turkey.
    Kabukcu S, Keskin N, Keskin A, Atalay E.
    Clin Appl Thromb Hemost; 2007 Apr; 13(2):166-71. PubMed ID: 17456626
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  • 12. The 19-bp deletion of dihydrofolate reductase (DHFR), methylenetetrahydrofolate reductase (MTHFR) C677T, Factor V Leiden, prothrombin G20210A polymorphisms in cancer patients with and without thrombosis.
    Eroglu A, Egin Y, Cam R, Akar N.
    Ann Hematol; 2009 Jan; 88(1):73-6. PubMed ID: 18682947
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  • 15. Contraception-related deep venous thrombosis and pulmonary embolism in a 17-Year-old girl heterozygous for factor V leiden, prothrombin G20210A mutation, MTHFR C677T and homozygous for PAI-1 mutation: report of a family with multiple genetic risk factors and review of the literature.
    Lenicek Krleza J, Jakovljevic G, Bronic A, Coen Herak D, Bonevski A, Stepan-Giljevic J, Roic G.
    Pathophysiol Haemost Thromb; 2010 Jan; 37(1):24-9. PubMed ID: 20664190
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  • 17. The influence of established genetic variation in the haemostatic system on clinical restenosis after percutaneous coronary interventions.
    Pons D, Monraats PS, de Maat MP, Pires NM, Quax PH, van Vlijmen BJ, Rosendaal FR, Zwinderman AH, Doevendans PA, Waltenberger J, de Winter RJ, Tio RA, Frants RR, van der Laarse A, van der Wall EE, Jukema JW.
    Thromb Haemost; 2007 Dec; 98(6):1323-8. PubMed ID: 18064331
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  • 18. The genetics of venous thromboembolism. A meta-analysis involving approximately 120,000 cases and 180,000 controls.
    Gohil R, Peck G, Sharma P.
    Thromb Haemost; 2009 Aug; 102(2):360-70. PubMed ID: 19652888
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  • 19. The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation.
    Margaglione M, D'Andrea G, d'Addedda M, Giuliani N, Cappucci G, Iannaccone L, Vecchione G, Grandone E, Brancaccio V, Di Minno G.
    Thromb Haemost; 1998 May; 79(5):907-11. PubMed ID: 9609218
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  • 20. Analysis of prothrombotic mutations and polymorphisms in children who developed thrombosis in the perioperative period of congenital cardiac surgery.
    Ozbek N, Ataç FB, Yildirim SV, Verdi H, Yazici C, Yilmaz BT, Tokel NK.
    Cardiol Young; 2005 Feb; 15(1):19-25. PubMed ID: 15831156
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