REFERENCES
- Baysal E, Carver MFH. The β- and δ-thalassemia repository (eighth edition). Hemoglobin. 1995;19(3–4):213–236.
- Patrinos GP, Giardine B, Riemer C, et al. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res. 2004;32(Database issue):D537-D541. http://globin.cse.psu.edu [].
- Hardison RC, Chui DHK, Giardine B, et al. HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server. Hum Mutat. 2002;19(3):225–233. http://globin.cse.psu.edu [].
- Abolghasemi H, Amid A, Zeinali S, . Thalassemia in Iran: epidemiology, prevention and management. J Pediatr Hematol Oncol. 2007;29(4):233–238.
- Samavat A, Modell B. Iranian national thalassaemia screening programme. BMJ. 2004;329(7475):1134–1137.
- Orkin SH, Kazazian HH, Antonarakis SE, . Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster. Nature. 1982;296(5858):627–631.
- Huisman THJ, Jonxis JHP. The Hemoglobinopathies Techniques of Identification. Clinical and Biochemical Analysis, Vol. 6. New York: Marcel Dekker, Inc. 1977.
- Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 1988;16(3):1215.
- Weatherall DJ, Clegg JB. The Thalassaemia Syndromes, 4th ed. Oxford: Blackwell, 2001.