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Thrombosis and Haemostasis|May 24, 2000
Major structural defects in the antithrombin gene in four families with type I antithrombin deficiency--partial/complete deletions and rearrangement of the antithrombin geneN J Beauchamp, M Makris, F E Preston, et al.
Thrombosis and Haemostasis|July 10, 1998
A novel mutation in intron K of the PROS1 gene causes aberrant RNA splicing and is a common cause of protein S deficiency in a UK thrombophilia cohortN J Beauchamp, M E Daly, M Makris, et al.
Thrombosis and Haemostasis|September 24, 1999
A common splice site mutation is shared by two families with different type 2N von Willebrand disease mutationsI M Nesbitt, K K Hampton, F E Preston, et al.
Thrombosis and Haemostasis|February 18, 1985
The application of a monoclonal antibody to factor VIII related antigen (VIIIRAg) in immunoradiometric assays for factor VIIIJ E Thomas, I R Peake, J C Giddings, et al.
British Journal of Haematology|January 1, 1989
Anti-idiotypes to factor VIII antibodies and their possible role in the pathogenesis and treatment of factor VIII inhibitorsE H Moffat, R A Furlong, A H Dannatt, et al.
British Journal of Urology|March 1, 1988
Development of a penile rigidity indicator and new concepts in the quantification of rigidityK M Desai, T J Floyd, D H Follett, et al.
Journal of Reproduction and Fertility|November 1, 1981
Temporal changes in rat Leydig cell function after the induction of bilateral cryptorchidismG P Risbridger, J B Kerr, R Peake, et al.
Clinical and Laboratory Haematology|January 1, 1980
Characterization of procoagulant activity produced by cultures of human monocytes and lymphocytes separated in colloidal silica-polvinylpyrrolidone gradientsJ C Giddings, F Piovella, M Ricetti, et al.
British Journal of Haematology|March 1, 1986
Comparison of phenotypic assessment and the use of two restriction fragment length polymorphisms in the diagnosis of the carrier state in haemophilia BD P Lillicrap, M B Liddell, R J Matthews, et al.
Blood|April 1, 1991
Cosegregation of von Willebrand factor gene polymorphisms and possible germinal mosaicism in type IIB von Willebrand diseaseE W Murray, A R Giles, P J Bridge, et al.
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