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Budd-chiari综合征患者凝血因子XVal34Leu基因多态性的检测 被引量:3

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出处 《中华血液学杂志》 CAS CSCD 北大核心 2005年第9期564-565,共2页 Chinese Journal of Hematology
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  • 1Lin GL, Xu PQ, Qi H, et al. Relations of Budd-Chiari syndrome to prothrombin gene mutation. Hepatobliary Pancreat Dis Int, 2004,3:173-175.
  • 2Kohler HP, Stickland MH, Ossei-Gerning N, et al. Association of a common polymorphism in the factor ⅩⅢ gene with myocardial infarction. Thromb Haemost. 1998,79: 8-13.
  • 3Franco RF, Pazin-Filho A, Tavella MH, et al. Factor ⅩⅢ val34leu and the risk of myocardial infarction. Haematologica, 2000, 85: 67-71.
  • 4Denninger MH,Chait Y, Casadevall N,et al. Cause of portal or hepatic venous thrombosis in adults:the role of multiple concurrent fators.Hepatology, 2000,31: 587 -591.
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  • 6Bertina RM, Koeleman BP, Koster T, et al. mutation in blood coagulation factor V associated with resistance to activated protein C. Nature, 1994, 369:64.
  • 7De Stefano V, Chiusolo P, Paciaroni K, et al. Prothrombin G20210Amutant genotype is a risk factor for cerebrovascular ischemic disease in young patients. Blood, 1998, 91:3562-3565.
  • 8Anwar R, Minford A, Gallivan L, et al. Delayed umibilical bleeding a pressing feature for factor ⅩⅢ deficiency: clinical features, genetics,and management. Pediatrics, 2002, 109: e32 .
  • 9Franco RF, Reitsma PH, Lourenco D,et al. Factor ⅩⅢ val34-to-leu is a genetic factor involved in the aetiology of venous thrombosis.Thromb Haemost, 1999, 81: 676-679.
  • 10Balogh I, Szoke G, Karpati L, et al. Val34Leu polymorphism of plasma factor ⅩⅢ: biochemistry and epidemiology in familial thrombophilia. Blood, 2000, 96: 2479-2486.

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