References
- Origa R, Paglietti ME, Sollaino MC, et al. Complexity of the α-globin genotypes identified with thalassemia screening in Sardinia. Blood Cells Mol Dis. 2014;52(1):46–49.
- Dehbozorgian J, Moghadam M, Daryanoush S, et al. Distribution of α-thalassemia mutations in Iranian population. Hematology. 2015;20(6):359–362.
- Galanello R, Cao A. Gene test review. α-thalassemia. Genet Med. 2011;13(2):83–88.
- Giordano PC, Bakker-Verwij M, Harteveld CL. Frequency of α-globin gene triplications and their interaction with β-thalassemia mutations. Hemoglobin. 2009;33(2):124–131.
- Goossens M, Dozy AM, Embury SH, et al. Triplicated α-globin loci in humans. Proc Natl Acad Sci USA. 1980;77(1):518–521.
- Moosavi SF, Amirian A, Zarbakhsh B, et al. The carrier frequency of α-globin gene triplication in an Iranian population with normal or borderline hematological parameters. Hemoglobin. 2011;35(4):323–330.
- Lie-Injo LE, Herrera AR, Kan YW. Two types of triplicated α-globin loci in humans. Nucleic Acids Res. 1981;9(15):3707–3717.
- Trent R, Higgs D, Clegg J, et al. A new triplicated α-globin gene arrangement in man. Br J Haematol. 1981;49(1):149–152.
- Camaschella C, Kattamis A, Petroni D, et al. Different hematological phenotypes caused by the interaction of triplicated α-globin genes and heterozygous β-thalassemia. Am J Hematol. 1997;55(2):83–88.
- Kimura E, Grignoli C, Pinheiro V, et al. Thalassemia intermedia as a result of heterozygosis for β0-thalassemia and ααα anti-3.7/αα genotype in a Brazilian patient. Braz J Med Biol Res. 2003;36(6):699–701.
- Farashi S, Bayat N, Faramarzi Garous N, et al. Interaction of an α-globin gene triplication with β-globin gene mutations in Iranian patients with β-thalassemia intermedia. Hemoglobin. 2015;39(3):201–206.
- Waye JS, Chui DHK. The α-globin gene cluster: genetics and disorders. Clin Invest Med. 2001;24(2):103–109.
- Moosavi A, Ardekani AM. The frequency and importance of common α-globin gene deletions among β-thalassemia carriers in an Iranian population. Avicenna J Med Biotechnol. 2017;9(4):196–200.
- Ma S, Au W, Chan A, et al. Clinical phenotype of triplicated α-globin genes and heterozygosity for β0-thalassemia in Chinese subjects. Int J Mol Med. 2001;8(2):171–175.
- Cebrian FY, Flores MVR, Álvarez SI, et al. Combination of a triple α-globin gene with β-thalassemia in a Gypsy family: importance of the genetic testing in the diagnosis and search for a donor for bone marrow transplantation for one of their children. BMC Res Notes. 2016;9(1):220–225.
- Wu M-Y, Zhou J-Y, Li J, et al. The frequency of α-globin gene triplication in a southern Chinese population. Indian J Hematol Blood Transfus. 2016;32(S1):320–322.
- Bragos I, Noguera N, Raviola M, et al. Triplication (/ααα anti3.7) or deletion (-α3.7/) association in Argentinian β-thalassemic carriers. Ann Hematol. 2003;82(11):696–698.
- Traeger-Synodinos J, Kanavakis E, Vrettou C, et al. The triplicated α globin gene locus in β thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies. Br J Haematol. 1996;95(3):467–471.
- Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucl Acids Res. 1988;16(3):1215
- Baysal E, Huisman T. Detection of common deletional α-thalassemia-2 determinants by PCR. Am J Hematol. 1994;46(3):208–213.
- Wang W, Ma ES, Chan AY, et al. Single-tube multiplex-PCR screen for anti-3.7 and anti-4.2 α-globin gene triplications. Clin Chem. 2003;49(10):1679–1682.
- Harteveld CL, Voskamp A, Phylipsen M, et al. Nine unknown rearrangements in 16p13.3 and 11p15.4 causing α- and β-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification. J Med Genet. 2005;42(12):922–931.
- Fisher CA, Premawardhena A, de Silva S, et al. The molecular basis for the thalassaemias in Sri Lanka. Br J Haematol. 2003;121(4):662–671.
- Nadkarni A, Phanasgaonkar S, Colah R, et al. Prevalence and molecular characterization of α-thalassemia syndromes among Indians. Genet Test. 2008;12(2):177–180.