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Sickle Cell Anemia Search result for 'Sickle Cell Anemia': Paper Excerpts: ... performance, through, for instance, verbally reacting aloud as one might in the African-American church tradition, or of advertising campaign to reflect "Destination Miller Time", but the company is not going to associate itself with the tradition. The play itself takes place over a single day in 1927, in a Chicago recording studio. The great blues singer Ma Rainey to the ideological power struggles of the various characters. The mixed, intercultural audience therefore has, as such, knowing what is `supposed' to happen along with the actors, as an audience watching a familiar folktale in the Noh ...
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Sources list for SICKLE CELL ANEMIA: Charache, et. al. 1995. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia. N Engl J Med 332:1317-22.Sickle Cell Disease Powars, D, et. al. 1994. Beta-S gene cluster haplotypes modulate hematologic and hemorheologic expression in sickle cell anemia. Use in predicting clinical severity. Am. J. Ped. Hematology-Oncology 16:55-61. Sickle Cell Disease Powars, D, et al. 1993. Sickle cell anemia. Beta s gene cluster haplotypes as genetic markers for severe disease expression. Am. J. Dis. Child. 147:1197-1202. Sickle Cell Disease Seltzer, WK; Abshire, TC; Lane, PA; Roloff, JS; Githens, JH. 1992. Molecular genetic studies in black families with sickle cell anemia and unusually high levels of fetal hemoglobin. Hemoglobin 16: 363-77. Sickle Cell Disease Kehinde MO, Akinsola FB. Ocular findings in sickle cell disease patients in lagos. Niger Postgrad Med J 2004;11:203-6. Sickle Cell Retinopathy More sources on "SICKLE CELL ANEMIA"
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