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Leukemia Research|October 1, 1994
Persistent polyclonal B-cell lymphocytosisS Agrawal, E Matutes, J Voke, et al.Journal of Clinical Pathology|December 1, 1977
Immune complexes and abnormal liver function in haemophiliaB A McVerry, J Voke, I Mohammed, et al.American Journal of Obstetrics and Gynecology|July 1, 1994
Erythropoietic suppression in fetal anemia because of Kell alloimmunizationJ I Vaughan, R Warwick, E Letsky, et al.British Journal of Haematology|January 1, 1992
Mononuclear phagocyte assays, autoanalyzer quantitation and IgG subclasses of maternal anti-RhD in the prediction of the severity of haemolytic disease in the fetus before 32 weeks gestationS F Garner, E Wiener, M Contreras, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1993
A novel point mutation (Val 297-->Met) in the serine proteinase domain of protein C in a patient with both venous and arterial thromboembolic diseaseD S Millar, A I Wacey, J Voke, et al.Clinical and Laboratory Haematology|November 13, 2001
The outcome of ambulatory DVT management using a multidisciplinary approachP Rose, D Bell, E S Green, et al.British Journal of Obstetrics and Gynaecology|December 1, 1983
Prolonged heparin therapy in pregnancy causes bone demineralizationM de Swiet, P D Ward, J Fidler, et al.Blood|May 1, 1996
Severe perinatal thrombosis in double and triple heterozygous offspring of a family segregating two independent protein S mutations and a protein C mutationC J Formstone, P J Hallam, E G Tuddenham, et al.Blood|October 1, 1995
Detection and characterization of seven novel protein S (PROS) gene lesions: evaluation of reverse transcript-polymerase chain reaction as a mutation screening strategyC J Formstone, A I Wacey, L P Berg, et al.Pageof 2