Apparent ‘dominant’ and ‘recessive’ inheritance of von Willebrand's disease within the same kindreds. Possible biochemical mechanisms
- 1 January 1979
- journal article
- research article
- Published by Elsevier in Thrombosis Research
- Vol. 15 (3-4) , 505-512
- https://doi.org/10.1016/0049-3848(79)90156-7
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
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- Willebrand Factor and Ristocetin II. RELATIONSHIP BETWEEN WILLEBRAND FACTOR, WILLEBRAND ANTIGEN AND FACTOR‐VIII ACTIVITYBritish Journal of Haematology, 1974
- Inherited Variants of Factor-VIII-Related Protein in von Willebrand's DiseaseNew England Journal of Medicine, 1974
- A Variant of Factor VIII Related AntigenBritish Journal of Haematology, 1974
- The presence and reactions of high and lower-molecular-weight procoagulant factor VIII in the plasma of patients with von Willebrand's disease after treatment: Significance for a structural hypothesis for factor VIIIThrombosis Research, 1973
- Detection of Heterozygotes for Recessive von Willebrand's Disease by the Assay of Antihemophilic-Factor-like AntigenNew England Journal of Medicine, 1973
- Genetic Variants of von Willebrand's DiseaseBMJ, 1972
- Assay of Plasma Antihaemophilic Globulin (AHG)*British Journal of Haematology, 1959