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Articles related to 14669613 [Unique ID], provided by the PubMed system
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Kapustin SI, Blinov MN, Kargin VD, et al. 
[Genetic determinants of hereditary thrombophilia in pathogenesis of venous thrombosis] [English Abstract, Journal Article]
Ter Arkh 2003; 75(10):78-80.
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Almawi WY, Tamim H, Kreidy R, et al. 
A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis. [Journal Article]
J Thromb Thrombolysis 2005 Jun; 19(3):189-96.
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Martinelli I, Battaglioli T, Razzari C, et al. 
Type and location of venous thromboembolism in patients with factor V Leiden, prothrombin G20210A and in those with no thrombophilia. [JOURNAL ARTICLE]
J Thromb Haemost 2006 Oct 25.
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Toydemir PB, Elhan AH, Tükün A, et al. 
Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behçet's disease. [Journal Article]
J Rheumatol 2000 Dec; 27(12):2849-54.
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Ivanov P, Komsa-Penkova R, Kovacheva K, et al. 
Impact of Thrombophilic Genetic Factors on Pulmonary Embolism: Early Onset and Recurrent Incidences. [JOURNAL ARTICLE]
Lung 2007 Dec 21.
Abstract | Full Citation
Nizankowska-Mogilnicka E, Adamek L, Grzanka P, et al. 
Genetic polymorphisms associated with acute pulmonary embolism and deep venous thrombosis. [Journal Article]
Eur Respir J 2003 Jan; 21(1):25-30.
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[C677T mutation in methylentetrahydrofolatereductase gene in patients with venous thromboses from the central region of Russia correlates with a high risk of pulmonary artery thromboembolism] [Journal Article]
Ter Arkh 2006; 78(6):70-6.
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Dölek B, Eraslan S, Eroğlu S, et al. 
Molecular analysis of factor V Leiden, factor V Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients. [Journal Article, Research Support, Non-U.S. Gov't]
Clin Appl Thromb Hemost 2007 Oct; 13(4):435-8.
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Dordević V, Rakićević L, Spasić M, et al. 
[Factor V Leiden, FII G20210A, MTHFR C677T mutations as risk factors for venous thrombosis during pregnancy and puerperium] [Journal Article]
Vojnosanit Pregl 2005 Mar; 62(3):201-5.
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