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Original Article

Rare Factor Vii Variant Inherited Through Genetic Variant in Proband'S Mother and Another Genetic Variant in Proband'S Father

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Pages 145-151 | Received 18 Aug 1986, Accepted 02 Feb 1987, Published online: 09 Jul 2009

References

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  • Roller F., Loeliger A., Duckert F. Experiments on a new clotting factor (factor VII). Acta Haematol 1951; 6: 1
  • Alexander B., Goldstein R., Landwehr G., Cook C. D. Congenital SPCA deficiency. A hitherto unrecognized defect with hemorrhage rectified by serum and serum factors. J Clin Invest 1951; 30: 596–606
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  • Goodnight S. H., Feinstein D. J., Østerud B., Rapaport S. I. Factor VII-antibody-neutralizing material in hereditary and acquired factor VII deficiency. Blood 1971; 38: 1–8
  • Mariani G., Mazzucconi M. G. Factor VII congenital deficiency. Clinical picture and classification of the variants. Haemostasis 1983; 13: 169–177
  • Triplett D. A., Brandt J. T., McGann Batarel M. A., Schaeffer Dixon J. L., Fair D. S. Hereditary factor VII deficiency: Heterogeneity defined by combined functional and immunochemical analysis. Blood 1985; 66: 1284–1287
  • Hall C. A., Rapaport S. I., Ames S. B. A clinical and family study of hereditary proconvertin (factor VII) deficiency. Am J Med 1964; 37: 172–181

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