References
- Modell B, Darlison M. Global epidemiology of haemoglobin disorders and derived service indicators. Bull World Health Organ 2008; 86: 480–487.
- Rahim F, Ahadi R. Thalassaemia and haemoglobin disorders in the Khuzestan Province of Iran. J Clin Diagn Res 2008; 3: 820–826.
- Cao A, Saba L, Galanello R, Rosatelli MC. Molecular diagnosis, and carrier screening for beta thalassemia. JAMA 1997; 278: 1273–1277.
- Lorey FW, Arnopp J, Cunningham GC. Distribution of hemoglo-binopathy variants by ethnicity in a multiethnic state. Genet Epidemiol 1996; 13: 501–512.
- Birgens HS, Karle H, Guldberg P, Guttler F. Hemoglobinopathy in the county of Copenhagen. Ugeskr Laeger 1997; 159: 3934–3939.
- Vetter B, Schwarz C, Kohne E, Kulozik AE. Beta-thalassaemia in the immigrant and non-immigrant German populations. Br J Haematol 1997; 97: 266–272.
- Rengelink-van der Lee JH, Schulpen TW, Beemer FA. Incidence and prevalence of hemoglobinopathies in children in The Netherlands. Ned Tijdschr Geneeskd 1995; 139: 1498–1501.
- Haghshenas M, Zamani J. Thalassemia. 1st ed. Shiraz: Shiraz University of Medical Sciences Publishing Center, 1997.
- Rahim F, Abromand M. Spectrum of beta-thalassemia mutationsin various Ethnic Regions of Iran. Pak J Med Sci 2008; 24: 410–415.
- Rahim F. Microcytic hypochromic anemia patients with thalasse-mia: genotyping approach. Indian J Med Sci 2009; 63: 101–108.
- Nishank SS, Ranjit M, Kar SK, Chhotray GP. Molecular variants and clinical importance of beta-thalassaemia traits found in the state of Orissa, India. Hematology 2009; 14: 290–296.
- Camaschella C, Bertero MT, Serra A et al. A benign form of thalassaemia intermedia may be determined by the interaction of triplicated alpha locus and heterozygous beta-thalassaemia. Br J Haematol 1987; 66: 103–107.
- Rahim F, Kaikhaei B, Zandian K, Hoseini A. Co-inheritance of alpha- and beta-thalassemia in Khuzestan Province, Iran. Hematology 2008; 13: 59–64.
- Rahim F, Kaeikhaei B, Akbari MT. Application of diagnostic methods and molecular diagnosis of hemoglobin disorders in Khuzestan province of Iran. Indian J Hum Genet 2007; 13: 5–15.
- Shokrani M, Terrell F, Turner EA, Aguinaga MD. Chromatographic measurements of hemoglobin A2 in blood samples that contain sickle hemoglobin. Ann Clin Lab Sci 2000; 30: 191–194.
- Betke K, Marti HR, Schlicht I. Estimation of small percentages of foetal haemoglobin. Nature 1959; 184(Suppl 24): 1877–1878.
- Rahim F, Keikhaei B. Better differential diagnosis of iron deficiency anemia from beta-thalassemia trait. Turk J Hematol 2009; 26: 138–145.
- Liu YT, Old JM, Miles K, Fisher CA, Weatherall DJ, Clegg JB. Rapid detection of alpha-thalassaemia deletions and alpha-globin gene triplication by multiplex polymerase chain reactions. Br J Haematol 2000; 108: 295–299.
- Kazazian HH, Jr, Dowling CE, Waber PG, Huang S, Lo WH. The spectrum of beta-thalassemia genes in China and Southeast Asia. Blood 1986; 68: 964–966.
- Najmabadi H, Pourfathollah AA, Neishabury M, Sahebjam F, Krugluger W, Oberkanins C. Rare and unexpected mutations among Iranian beta-thalassemia patients and prenatal samples discovered by reverse-hybridization and DNA sequencing. Haematologica 2002; 87: 1113–1114.
- Nozari G, Rahbar S, Golshaiyzan A, Rahmanzadeh S. Molecular analysis of beta- thalassemia in Iran. Hemoglobin 1995; 19: 425–431.
- Karimi M, Yarmohammadi H, Farjadian S et al. Beta-thalassemia intermedia from southern Iran: IVS-II-1 (G—>A) is the prevalent thalassemia intermedia allele. Hemoglobin 2002; 26: 147–154.