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American Journal of Clinical Pathology|August 1, 1980
Malignant histiocytosis simulating granulomatous diseaseR A Sacher, R J Jacobson, B A Lenes, et al.Vox Sanguinis|January 1, 1975
Double heterozygosity for hemoglobin Camden (beta 131 Gln yields Glu) and hemoglobin S in an American negroR Q Blackwell, P R McCurdy, C S Liu, et al.Journal of Clinical Apheresis|January 1, 1983
Complications related to equipment and techniqueH G Klein, P R McCurdy, H G Braine, et al.The Journal of Biological Chemistry|December 10, 1976
Hemoglobin providence. Functional consequences of two alterations of the 2,3-diphosphoglycerate binding site at position beta 82J Bonaventura, C Bonaventura, B Sullivan, et al.American Journal of Clinical Pathology|March 1, 1982
The occurrence of an auto-immune hemolytic anemia with anti-U specificity in a patient with myelodysplastic syndromeR A Sacher, M M McGinniss, G G Shashaty, et al.JAMA|September 27, 2001
Prevalence, donation practices, and risk assessment of blood donors with hemochromatosisA M Sanchez, G B Schreiber, J Bethel, et al.Transfusion|July 1, 1977
The in vivo survival of red blood cells stored in modified CPD with adenine: report of a multi-institutional cooperative effortT F Zuck, T A Bensinger, C C Peck, et al.Journal of Hematotherapy|January 27, 1999
Cord Blood Transplantation Study (COBLT): cord blood bank standard operating proceduresJ K Fraser, M S Cairo, E L Wagner, et al.Transfusion|September 30, 1999
Absence of human T-lymphotropic virus type I tax sequences in a population of normal blood donors in the Baltimore, MD/Washington, DC, area: results from a multicenter studyE P Cowan, G J Nemo, A E Williams, et al.Pageof 3