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Organization of α-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, β-thalassemia, and α-thalassemia-2

✍ Scribed by A. E. Felice; R. Ozdonmez; M. E. Headlee; T. H. J. Huisman


Publisher
Springer
Year
1982
Tongue
English
Weight
698 KB
Volume
20
Category
Article
ISSN
0006-2928

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## Abstract The in vitro synthesis of hemoglobin chains was investigated in 34 scikle cell anemia (SS) patients and five patients with Hb S‐β^o^‐thalassemia. Incubations were made for 30 minutes and for 120 minutes. Hematological and family data were also obtained. Although the 30‐minute α/non‐α to