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British Journal of Haematology|May 1, 1975
Alpha thalassaemia in adults with sickle-cell traitM H Steinberg, J G Adams, B J DreilingBritish Journal of Haematology|August 1, 1990
Isolation and characterization of the translation product of a beta-globin gene nonsense mutation (beta 121 GAA----TAA)J G Adams, M H Steinberg, H H KazazianAmerican Journal of Hematology|January 1, 1977
Sickle cell anemia: erythrokinetics, blood volumes, and a study of possible determinants of severityM H Steinberg, B J Dreiling, W J LovellThe Journal of Laboratory and Clinical Medicine|October 1, 1982
Beta-thalassemia with exceptionally high hemoglobin A2. Differential expression of the delta-globin gene in the presence of beta-thalassemiaM H Steinberg, M B Coleman, J G AdamsThe New England Journal of Medicine|October 22, 1987
Plasma glycocalicin. An aid in the classification of thrombocytopenic disordersM H Steinberg, J G Kelton, B S CollerThe Journal of Biological Chemistry|March 25, 1991
Hemoglobin Terre Haute arginine beta 106. A posthumous correction to the original structure of hemoglobin IndianapolisM B Coleman, M H Steinberg, J G AdamsMethods of Information in Medicine|February 1, 1997
Development of an HIV clinical and research database for South AfricaA S Kanter, D C Spencer, M H SteinbergBlood|November 1, 1981
Modulation of erythrocyte-endothelial interactions and the vasocclusive severity of sickling disordersR P Hebbel, C F Moldow, M H SteinbergProgress in Clinical and Biological Research|January 1, 1981
Erythrocyte calcium abnormalities in sickle cell diseaseR P Hebbel, M H Steinberg, J W EatonScience (New York, N.Y.)|October 15, 1982
Hemoglobin Parchman: double crossover within a single human geneJ G Adams, W T Morrison, M H SteinbergPageof 20