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Original Article

Combined Deficiency of Coagulation Factors Ii, Vii, IX, and X: A Case of Probable Congenital Origin

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Pages 187-193 | Received 06 Jan 1986, Accepted 26 Feb 1986, Published online: 09 Jul 2009

References

  • McMillan C W, Roberts H R. Congenital combined deficiency of coagulation factors II, VII, IX and X. N Engl J Med 1966; 274: 1313–1315
  • Chung K S, Bezeaud A, Goldsmith J C. Congenital deficiency of blood clotting factors II, VII, IX, and X. Blood 1979; 53: 776–787
  • Nilsson I M. Haemorrhagic and Thrombotic Diseases. John Wiley & Sons, London 1974
  • Ganrot P O, Niléhn J-E. Immunochemical determination of human prothrombin. Scan J Clin Lab Invest 1968; 21: 238–244
  • Klippel A P, Pitzinger B. Hypoprothrombinemia secondary to antibiotic therapy and manifested by massive gastrointestinal hemorrhage. Arch Surg 1968; 96: 266–268
  • Johnson C A, Chung K S, McGrath K M. Characterization of a variant prothrombin in a patient congenitally deficient in factors I, VII, IX and X. Br J Haematol 1980; 44: 461–469
  • Goldsmith G H, Pence R E, Ratnoff O D. Studies on a family with combined functional deficiencies of vitamin K-dependent coagulation factors. J Clin Invest 1982; 69: 1253–1260
  • Fischer M, Zweymuller E. Kongenitaler kombinierter Mangel der Faktoren II, VII und X. Z Kinderheilk 1966; 95: 309–323

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