Publisher
Springer Berlin Heidelberg
Reference5 articles.
1. Lechler E, Webster WP, Roberts HR, Penick GD (1965) The inheritance of Stuart disease: Investigation of a family with factor X deficiency. Amer J Med Sci 249: 291
2. McMillan CW, Roberts HR (1966) Congenital combined deficiency of coagulation factors II, VII, IX and X. New Engl J Med 274: 1313
3. Chung KS, Bezeaud A, Goldsmith JC, McMillan CW, MénachéD, Roberts HR (1979) Congenital deficiency of blood coagulation factors II, VII, IX and X. Blood 53: 776
4. Johnson CA, Chung KS, McGrath KM, Bean PE, Roberts HR (1980) Characterization of a variant Prothrombin in a patient congengenitally deficient in factors II, VII, IX and X. Brit J Haematol 44: 461
5. Roberts HR, Zeitler KD (1982) Inherited disorders of Prothrombin conversion. In: Colman RW, Hirsh J, Marder VJ, Salzman EW (eds) Hemostasis and thrombosis. JB Lippincot Company, Philadelphia and Toronto, p 127