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On the structure of the hemoglobins A, A2, and F in a Negro with homozygous β-thalassemia

✍ Scribed by W.A. Schroeder; T.H.J. Huisman; J.Roger Shelton; Gerald Apell; Joan B. Shelton; Anne R. Brodie; C.L. Luicher; M.H. Blunt; A. Miller

Book ID
115766280
Publisher
Elsevier Science
Year
1974
Tongue
English
Weight
958 KB
Volume
10
Category
Article
ISSN
0006-2944

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✍ Tadmouri, G. O.; Yüksel, L.; Başak, A. N. 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 36 KB 👁 1 views

␤-thalassemia and sickle cell disease (SCD) are common disorders in Turkey. Compound heterozygosity for these two disorders (␤ S /␤-thalassemia) is encountered frequently. In this report we present hematological and molecular data of two Turkish siblings with ␤ S /␤ del -thalassemia caused by a 290