REFERENCES
- Loutradi-Anagnostou A. Prevention of thalassemia in Greece: 25 year experience. The 8th International Conference on Thalassaemia and Haemoglobinopathies, AthensGreece, October, 2001. Abstract Book, 16–18
- Boussiou M, Karababa Ph, Sinopoulou K, Tsaftaridis P, Plata E, Loutradi-Anagnostou A. The molecular heterogeneity of β-thalassemia in Greece. Blood Cells Mol Dis 2008; 40(3)317–319
- Nathan D. Thalassemia: the continued challenge. Ann NY Acad Sci 2005; 1054: 1–10
- Papadopoulos V, Vassiliadou D, Xanthopoulidis G, Petridis D, Agorasti A, Loukopoulos D. The implications of Haemoglobin O-Arab mutation. Haematologica 2003; 90(2)255–257
- Weatherall DJ, Clegg JB. The Thalassaemia Syndromes4th. Blackwell Science, Oxford 2001
- Kaltsoya A, Ballas A, Sofroniadou K, Fessas Ph. A mild β-thalassemia-Hemoglobin E disease. The 5th Congress of the Asian and Pacific Society of Haematology, IstanbulTurkey, September, 1969. Abstract Book, 40
- Fessas Ph. Compound heterozygosity for Hb E-Saskatoon and β-thalassemia. Hemoglobin 1991; 15(4)35–346
- Theodoridou S, Plata E, Karababa Ph, Loutradi A, Vyzantiadis T, Manitsa A. The first case of a compound heterozygosity for Hb E-Saskatoon and Hb S. Haematologica 2003; 88(3)ECR08
- Tsistrakis GA, Scampardonis GJ, Clonizakis JP, Concouris LL. Haemoglobin D and β thalassaemia. A family report comprising 18 members. Acta Haematol 1975; 54(3)172–179
- Sinopoulou K, Lalou E, Karababa Ph, Bousiou M, Papadakis M, Theodoridou S, Karafoulidou A. A new β0 mutation, CD7 (G>T) in an Albanian. First report in the literature. 17th Panhellenic Haematological Congress, AthensGreece, November, 2006. Abstract Book, 78–79