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Archives of Pathology & Laboratory Medicine|June 1, 1987
Erythroblast multinuclearity in bone marrow and spleen. Congenital dyserythropoietic anemia-like abnormalities without functional evidence of dyserythropoiesisD P Lillicrap, W E Corbett, A R Giles, et al.Journal of Clinical Pathology|July 1, 1993
Sensitivity of PCR in detecting monoclonal B cell proliferationsF C Ling, C E Clarke, W E Corbett, et al.American Journal of Clinical Pathology|June 1, 1990
Heterogeneity of laboratory test results for antiphospholipid antibodies in patients treated with chlorpromazine and other phenothiazinesD P Lillicrap, M Pinto, K Benford, et al.British Journal of Haematology|June 1, 1989
Defective propeptide processing and abnormal activation underlie the molecular pathology of factor IX Troed-y-RhiwM B Liddell, D P Lillicrap, I R Peake, et al.American Journal of Hematology|November 1, 1987
Carrier detection in the hemophiliasD P Lillicrap, B N White, J J Holden, et al.British Journal of Haematology|May 8, 1999
Risk of venous thromboembolism associated with the common hereditary haemochromatosis Hfe gene (C282Y) mutationK Brown, R Luddington, S A Taylor, et al.American Journal of Hematology|June 1, 1993
Lymphoproliferative disease of "LAK cell" precursor large granular lymphocytes in association with celiac diseaseP Lopez, D G Morris, P R Galbraith, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|October 14, 2004
What is a cure and how do we get there?M W Skinner, D P Lillicrap, J McMillan, et al.Thrombosis and Haemostasis|January 23, 1992
Characterization of the original Christmas disease mutation (cysteine 206----serine): from clinical recognition to molecular pathogenesisS A Taylor, J Duffin, C Cameron, et al.Human Genetics|May 1, 1992
Differential termination of primer extension: a novel, quantifiable method for detection of point mutationsD J Picketts, C Cameron, S A Taylor, et al.Pageof 4