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Hematologic studies on patients with sickle cell anemia following multiple transfusions

✍ Scribed by Charles C. Donegan Jr.; William A. MacIlwaine; Byrd S. Leavell


Book ID
115673945
Publisher
Elsevier Science
Year
1954
Tongue
English
Weight
545 KB
Volume
17
Category
Article
ISSN
1555-7162

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## Abstract The diseases commonly confused with sickle cell anemia include sickle cellβ‐thalassemia in which synthesis of Ξ²^A^‐chains are completely suppressed (HbS‐β^O^‐thalassemia). We obtained hematologic measurements and studied globin biosynthesis in five patients with this disorder and compar