REFERENCES
- Weatherall DJ, Clegg JB, Higgs DR, Wood WG. The hemoglobinopathies. The Metabolic and Molecular Bases of Inherited Disease8th, CR Scriver. McGraw-Hill, New York 2001; 4571–4636
- Kazazian HH, Boehm CD. Molecular basis and prenatal diagnosis of β-thalassemia. Blood. 1988; 72(4)1107–1116
- Merat A, Haghshenas M, Mostafavi Pour Z, et al. β-Thalassemia in southwestern Iran. Hemoglobin. 1993; 17(5)427–437
- Yavarian M, Harteveld CL, Batelaan D, Bernini LF, Giordano PC. Molecular spectrum of β-thalassemia in the Iranian Province of Hormozgan. Hemoglobin. 2001; 25(1)35–34
- Najmabadi H, Karimi-Nejad R, Sahebjam S, et al. The β-thalassemia mutation spectrum in the Iranian population. Hemoglobin. 2001; 25(3)285–296
- Kiani AA, Mortazavi Y, Zeinali S, Shirkhani Y. The molecular analysis of β-thalassemia mutations in Lorestan Province, Iran. Hemoglobin. 2007; 31(3)343–349
- Derakhshandeh-Peykar P, Akhavan-Niaki H, Tamaddoni A, et al. Distribution of β-thalassemia mutations in the northern provinces of Iran. Hemoglobin. 2007; 31(3)351–356
- Hosseinpour Feizi MA, Hosseinpour Feizi AA, Pouladi N, Haghi M, Azarfam P. Molecular spectrum of β-thalassemia mutations in Northwestern Iran. Hemoglobin. 2008; 32(3)255–261
- Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cell. Nucleic Acids Res. 1988; 16(3)1215
- Rund D, Cohen T, Filon D, Dowling CE, Warren TC, Barak I. Evaluation of a genetic disease in an ethnic isolate: β-thalassemia in the Jews of Kurdistan. Proc Natl Acad Sci USA. 1991; 88(1)310–314
- Al-Allawi NAS, Jubrael JMS, Hughson M. Molecular characterization of β-thalassemia in the Dohuk region of Iraq. Hemoglobin. 2006; 30(4)479–486
- Ince HH, Ayyildiz O, Kalkanli S, Batun S, Muftuoglu E. Molecular basis of β-thalassemia mutations in Diyarbakir in the southeastern region of Turkey. Hemoglobin. 2003; 27(4)275–278
- Chakrabarti P, Gupta R, Mishra A, Rai M, Singh VP, Dash D. Spectrum of β-thalassemia mutations in North Indian states. A β-thalassemia trait with two mutations in cis. Clin Biochem. 2005; 38(6)576–578
- Suhaib A, Petrou M, Saleem M. Molecular genetics of β-thalassaemia in Pakistan: a basis for prenatal diagnoses. Br J Haematol. 1996; 94(3)476–482
- Kazazian HH, Jr. The thalassemia syndromes: molecular basis and prenatal diagnosis in 1990. Semin Hematol. 1990; 27(3)209–228
- Tadmouri GO, Tuzmen S, Ozcelik H, et al. Molecular and population genetic analyses of β-thalassemia in Turkey. Am J Hematol. 1998; 57(3)215–220
- Girodon E, Ghanem N, Vidaud M, et al. Rapid molecular characterization of mutations leading to unstable hemoglobin β-chain variants. Ann Hematol. 1992; 65(4)188–192
- Orkin SH, Kazazian HH, Antonarakis SE, et al. Linkage of β-thalassaemia mutation and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster. Nature. 1982; 296(5858)627–631