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RESEARCH PAPER ABOUT SICKLE CELL ANEMIA Definition by WordNet

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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

 

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RESEARCH PAPER ABOUT SICKLE CELL ANEMIA essays

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Sickle Cell Disease
This paper deals with sickle-cell disease (SCD, also known as sickle cell anemia) from a genetic point of view. -- 1,400 words; 8 sources;
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Sickle Cell Anemia
An analysis of sickle cell anemia, an inherited blood disorder of defective hemoglobin. -- 1,065 words; 8 sources; MLA
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Sickle Cell Anemia
An in-depth look at sickle cell anemia. -- 2,929 words; 13 sources; MLA
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Sickle-Cell Anemia
A case study of a 37-year old African-American male with a diagnosed case of sickle-cell anemia. -- 1,024 words; 3 sources; MLA
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Biochemistry and Genetics of Sickle-Cell Anemia
Presents an overview of sickle-cell anemia, looking at current treatment of the disease, its prognosis and promising treatments on the horizon. -- 1,800 words; 9 sources;
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