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British Journal of Haematology|April 1, 1989
Myelofibrosis in primary myelodysplastic syndromes: a clinico-morphological study of 10 casesA Pagliuca, D M Layton, A Manoharan, et al.International Journal of Molecular Medicine|December 19, 1998
Quantification of Ggamma- and Agamma-globins by electrospray ionisation mass spectrometryS F Ofori-Acquah, B N Green, B J Wild, et al.Blood|October 15, 1996
Two novel mutations in the reduced nicotinamide adenine dinucleotide (NADH)-cytochrome b5 reductase gene of a patient with generalized type, hereditary methemoglobinemiaJ Manabe, R Arya, H Sumimoto, et al.Obstetric Medicine|September 1, 2016
Pregnancy outcomes in sickle cell disease: a retrospective cohort study from two tertiary centres in the UKA R Chase, M Sohal, J Howard, et al.Blood Cells, Molecules & Diseases|November 29, 2005
Identification and characterization of the novel FAD-binding lobe G75S mutation in cytochrome b(5) reductase: an aid to determine recessive congenital methemoglobinemia status in an infantM J Percy, L J Crowley, D Roper, et al.Archives of Disease in Childhood|April 1, 1992
Blood leucocyte count in the human fetusN P Davies, A G Buggins, R J Snijders, et al.Archives of Disease in Childhood|April 1, 1992
Fetal leucocyte count in rhesus diseaseN P Davies, A G Buggins, R J Snijders, et al.British Journal of Haematology|December 1, 1994
Haemophagocytic lymphohistiocytosis: experience at two U.K. centresW J Hirst, D M Layton, S Singh, et al.Analytical Biochemistry|October 25, 2001
Mass spectral analysis of asymmetric hemoglobin hybrids: demonstration of Hb FS (alpha2gammabetaS) in sickle cell diseaseS F Ofori-Acquah, B N Green, S C Davies, et al.British Journal of Haematology|October 1, 1990
Clinicopathological features of acute undifferentiated leukaemia with a stem cell phenotypeF Brito-Babapulle, H Pullon, D M Layton, et al.Pageof 5