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Lancet (London, England)|April 16, 1994
Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuriaM Bessler, P Mason, P Hillmen, et al.The Journal of Biological Chemistry|May 25, 1976
Genetic variants of human erythrocyte glucose-6-phosphate dehydrogenase. Kinetic and thermodynamic parameters of variants A, B, and A- in relation to quaternary structureA O Babalola, J G Beetlestone, L LuzzattoBlood|January 1, 1993
Production and characterization of lymphoblastoid cell lines with the paroxysmal nocturnal hemoglobinuria phenotypeP Hillmen, M Bessler, D H Crawford, et al.Leukemia & Lymphoma|July 28, 2016
Rearrangement of T-cell Receptor (Delta, Gamma and Beta) Genes and its Significance in T-cell Chronic LeukaemiasA K Singh, M Laffan, S Eridani, et al.Journal of Medical Genetics|July 1, 1993
Dyskeratosis congenita: three additional families show linkage to a locus in Xq28R Arngrimsson, I Dokal, L Luzzatto, et al.Clinical and Laboratory Haematology|January 1, 1983
Familial erythrocytosis with over-production of erythropoietinA Hellmann, B Rotoli, P M Cotes, et al.British Journal of Haematology|August 1, 1994
Mutations in the PIG-A gene causing partial deficiency of GPI-linked surface proteins (PNH II) in patients with paroxysmal nocturnal haemoglobinuriaM Bessler, P J Mason, P Hillmen, et al.Blood|October 1, 1975
Glucose 6-phosphate dehydrogenase deficiency and sickle cell anemia: frequency and features of the association in an African communityU Bienzle, O Sodeinde, C E Effiong, et al.Molecular Biology & Medicine|February 1, 1984
DNA rearrangements of immunoglobulin genes correlate with phenotypic markers in B-cell malignanciesL Foroni, D Catovsky, T H Rabbitts, et al.Blood|October 27, 1998
New somatic mutation in the PIG-A gene emerges at relapse of paroxysmal nocturnal hemoglobinuriaK Nafa, M Bessler, H J Deeg, et al.Pageof 21