Showing results (1-10 of 33) with videos related to
Sort By:
Pageof 4
American Journal of Medical Genetics|May 1, 1989
Molecular diagnosis of the fragile X [Fra (X)] syndrome: calculation of risks based on flanking DNA markers in small phase-unknown familiesP J Bridge, D P LillicrapBritish Journal of Haematology|January 1, 1986
Prolonged thrombocytopenia in post-transfusion purpura (PTP) associated with changes in the crossed immunoelectrophoretic pattern of von Willebrand factor (vWF), circulating immune complexes and endothelial cell cytotoxicityD P Lillicrap, P M Ford, A R GilesThe Journal of Rheumatology|April 1, 1988
Association of lupus anticoagulant with severe valvular heart disease in systemic lupus erythematosusP M Ford, S E Ford, D P LillicrapAmerican Journal of Medical Genetics|March 15, 1991
Carrier detection and prenatal diagnosis of Pelizaeus-Merzbacher disease using a combination of anonymous DNA polymorphisms and the proteolipid protein (PLP) gene cDNAP J Bridge, P M MacLeod, D P LillicrapAmerican Journal of Hematology|September 1, 1999
Multicentric warfarin-induced skin necrosis complicating heparin-induced thrombocytopeniaT E Warkentin, W M Sikov, D P LillicrapProceedings of the National Academy of Sciences of the United States of America|January 1, 1991
Somatic mosaicism and female-to-female transmission in a kindred with hemophilia B (factor IX deficiency)S A Taylor, K V Deugau, D P LillicrapNature Genetics|February 1, 1993
Synergy between transcription factors DBP and C/EBP compensates for a haemophilia B Leyden factor IX mutationD J Picketts, D P Lillicrap, C R MuellerThe Quarterly Journal of Medicine|April 1, 1986
Inherited thrombocytopenia, elevated serum IgA and renal disease: identification as a variant of the Wiskott-Aldrich syndromeG R Standen, D P Lillicrap, N Matthews, et al.Stroke|January 1, 1990
Premature stroke in a family with lupus anticoagulant and antiphospholipid antibodiesP M Ford, D Brunet, D P Lillicrap, et al.Journal of Inherited Metabolic Disease|January 1, 1992
Gonadal mosaicism in a family with adrenoleukodystrophy: molecular diagnosis of carrier status among daughters of a gonadal mosaic when direct detection of the mutation is not possibleG E Graham, P M MacLeod, D P Lillicrap, et al.Pageof 4