We have analyzed the hemoglobin abnormalities in nearly 50 Albanian patients with a significant hemoglobinopathy and included 37 relatives in this study. Sickle cell anemia (SS) is a common disorder; all 15 sickle cell anemia patients had the complications expected for this disease. The beta S haplo
✦ LIBER ✦
Sickle Cell Thalassemia in Greece : Identification and Contribution of the Interacting β-Thalassemia Gene
✍ Scribed by ERSI VOSKARIDOU; PANAGOULA KOLLIA; DIMITRIS LOUKOPOULOS
- Book ID
- 119864581
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 92 KB
- Volume
- 612
- Category
- Article
- ISSN
- 0890-6564
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