The Combination of HB S and HB E in a Black Female
Author:
Affiliation:
1. Laboratory of Protein Chemistry and Comprehensive Sickle Cell Center, Medical College of Georgia, Augusta, Ga, 30902, USA
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
https://www.tandfonline.com/doi/pdf/10.3109/03630267609031026
Reference6 articles.
1. The First Observation of Sickle-Cell Hæmoglobin E Disease
2. The Hemoglobin E Syndromes. II. Sickle-Cell—Hemoglobin E Disease
3. Abraham E. C., Reese A., Stallings H., Huisman T. H.J., this issue.
4. Haemoglobin E and alpha-Thalassaemia.
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