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American Journal of Hematology|January 1, 1976
Clinical, hematologic and biosynthetic studies in sickle cell-betao-thalassemia: a comparison with sickle cell anemiaM H Steinberg, B J DreilingBlood Cells, Molecules & Diseases|August 1, 1997
Fetal hemoglobin in sickle cell anemia: examination of phylogenetically conserved sequences within the locus control region but outside the cores of hypersensitive sites 2 and 3M S Figueiredo, M H SteinbergAmerican Journal of Hematology|February 1, 1982
Thalassemia: recent insights into molecular mechanismsM H Steinberg, J G AdamsProgress in Clinical and Biological Research|January 1, 1981
Low output hemoglobins which produce the phenotype of thalassemiaJ G Adams, M H SteinbergBlood|February 15, 1996
Fetal hemoglobin in sickle cell anemia: relation to regulatory sequences cis to the beta-globin gene. Multicenter Study of HydroxyureaZ H Lu, M H SteinbergBlood|November 1, 1986
Alpha-thalassemia in blacks: genetic and clinical aspects and interactions with the sickle hemoglobin geneM H Steinberg, S H EmburyJournal of the American Geriatrics Society|January 1, 1983
Red blood cell glucose-6-phosphate dehydrogenase activity in aged humansG P Rodgers, H C Lichtman, M F SheffThe American Journal of Pediatric Hematology/Oncology|January 1, 1985
Noninvasive techniques to evaluate the vaso-occlusive manifestations of sickle cell diseaseG P Rodgers, C T Noguchi, A N SchechterProgress in Clinical and Biological Research|January 1, 1987
The development of non-invasive methods to evaluate sickle cell patients in the steady state and in crisisG P Rodgers, C T Noguchi, A N SchechterPageof 20