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Proceedings of the National Academy of Sciences of the United States of America|February 1, 1979
Genetic heterogeneity of "normal" human erythrocyte glucose-6-phosphate dehydrogenase: an isoelectrophoretic polymorphismG Modiano, G Battistuzzi, G J Esan, et al.
Journal of Internal Medicine|January 1, 1994
Tissue plasminogen activator for hepatic vein thrombosis in paroxysmal nocturnal haemoglobinuriaM F McMullin, P Hillmen, J Jackson, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 9, 1982
Pyruvate kinase deficiency: characterization of two new genetic variantsL Dente, M D'Urso, S Di Maio, et al.
The Journal of Laboratory and Clinical Medicine|May 1, 1979
Genetically determined deficiency of glucose 6-phosphate dehydrogenase (type-A-) is expressed in the liverO A Oluboyede, G J Esan, T I Francis, et al.
Blood Cells, Molecules & Diseases|October 29, 1998
The spectrum of somatic mutations in the PIG-A gene in paroxysmal nocturnal hemoglobinuria includes large deletions and small duplicationsK Nafa, M Bessler, H Castro-Malaspina, et al.
Journal of Virology|April 25, 2000
The cHS4 insulator increases the probability of retroviral expression at random chromosomal integration sitesS Rivella, J A Callegari, C May, et al.
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