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Molecular Analysis of Beta-Thalassemia and Sickle Cell Anemia in Antalya

✍ Scribed by Keser, I.; Sanlioglu, A.D.; Manguoglu, E.; Guzeloglu Kayisli, O.; Nal, N.; Sargin, F.; Yesilipek, A.; Simsek, M.; Mendilcioglu, I.; Canatan, D.

Book ID
111912662
Publisher
S. Karger AG
Year
2004
Tongue
English
Weight
61 KB
Volume
111
Category
Article
ISSN
0001-5792

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Sickle cell anemia, sickle cell Ξ²-thalas
Sickle cell anemia, sickle cell Ξ²-thalassemia, and thalassemia major in Albania: characterization of mutations
✍ Enis Boletini; Martina Svobodova; Vladimir Divoky; Erol Baysal; Mehmet A. CΓΌrΓΌk; πŸ“‚ Article πŸ“… 1994 πŸ› Springer 🌐 English βš– 569 KB

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