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The Quarterly Journal of Medicine|March 1, 1986
The importance of anaemia in cerebral and uncomplicated falciparum malaria: role of complications, dyserythropoiesis and iron sequestrationR E Phillips, S Looareesuwan, D A Warrell, et al.British Medical Journal|July 26, 1980
Haemoglobin Bart's hydrops syndrome in GreeceC Kattamis, A Metaxotou-Mavromati, E Tsiarta, et al.British Journal of Haematology|February 1, 1977
Haemoglobin Radcliffe (alpha2beta299(Gi)Ala): a high oxygen-affinity variant causing familial polycythaemiaD J Weatherall, J B Clegg, S T Callender, et al.Lancet (London, England)|June 8, 1985
Rearrangement of the T-cell-receptor beta-chain gene in the diagnosis of lymphoproliferative disordersN T O'Connor, J S Wainscoat, D J Weatherall, et al.Blood|February 1, 1986
Alpha thalassemia and the hematology of homozygous sickle cell disease in childhoodM C Stevens, G H Maude, M Beckford, et al.QJM : Monthly Journal of the Association of Physicians|April 16, 1998
Plasmodium vivax: a cause of malnutrition in young childrenT N Williams, K Maitland, L Phelps, et al.American Journal of Human Genetics|May 1, 1977
Inheritance of F cell frequency in heterocellular hereditary persistence of fetal hemoglobin: an example of allelic exclusionS H Boyer, L Margolet, M L Boyer, et al.Proceedings of the National Academy of Sciences of the United States of America|May 1, 1990
Molecular basis for dominantly inherited inclusion body beta-thalassemiaS L Thein, C Hesketh, P Taylor, et al.Proceedings of the National Academy of Sciences of the United States of America|May 23, 2007
Age-related changes in adaptation to severe anemia in childhood in developing countriesAngela O'Donnell, A Premawardhena, M Arambepola, et al.Lancet (London, England)|October 7, 1989
Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic diseaseJ Lamb, A O Wilkie, P C Harris, et al.Pageof 27