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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.
Thorax|July 20, 2018
Change in biomarkers of type-2 inflammation following severe exacerbations of asthmaRuth Semprini, Nick Shortt, Stefan Ebmeier, 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.
Blood|September 25, 2004
UGT1A1 variation and gallstone formation in sickle cell diseaseEden V Haverfield, Colin A McKenzie, Terrence Forrester, 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.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 20, 2008
Secondary prophylaxis with recombinant activated factor VII improves health-related quality of life of haemophilia patients with inhibitorsW K Hoots, L S Ebbesen, B A Konkle, 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.
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