References
- Farra C, Daher R, Badra R, et al. Incidence of alpha-globin gene defect in the Lebanese population: a pilot study. Biomed Res Int. 2015;2015:517679. doi: 10.1155/2015/517679.
- Shen X, Xu Y, Zhong Y, et al. Preimplantation genetic diagnosis for α- and β-double thalassemia. J Assist Reprod Genet. 2011;28(10):957–964.
- Bozdogan ST, Yuregir OO, Buyukkurt N, et al. α-Thalassemia mutations in Adana Province, southern Turkey: genotype-phenotype correlation. Indian J Hematol Blood Transfus. 2015;31(2):223–228.
- Oron-Karni V, Filon D, Shifrin Y, et al. Diversity of α-globin mutations and clinical presentation of α-thalassemia in Israel. Am J Hematol. 2000;65(3):196–203.
- Traeger-Synodinos J. Molecular basis of α-thalassaemia. Thalassemia Rep. 2012;1(s2):e13. doi: 10.4081/thal.2011.s2.e13.
- Galanello R, Cao A. Gene test review. α-Thalassemia. Genet Med. 2011;13(2):83–88.
- Akhavan-Niaki H, Youssefi Kamangari R, Banihashemi A, et al. Hematologic features of α-thalassemia carriers. Int J Mol Cell Med. 2012;1(3):162–167.
- 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.
- Tan ASC, Quah TC, Low PS, Chong SS. A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for α-thalassemia. Blood. 2001;98(1):250–251.
- Foglietta E, Bianco I, Maggio A, Giambona A. Rapid detection of six common Mediterranean and three non-Mediterranean α-thalassemia point mutations by reverse dot blot analysis. Am J Hematol. 2003;74(3):191–195.
- Chong SS, Boehm CD, Cutting GR, Higgs DR. Simplified multiplex-PCR diagnosis of common Southeast Asian deletional determinants of α-thalassemia. Clin Chem. 2000;46(10):1692–1695.
- Foglietta E, Deidda G, Graziani B, et al. Detection of alpha-globin gene disorders by a simple PCR methodology. Haematologica. 1996;81:387–396.
- Harteveld CL, Yavarian M, Zorai A, et al. Molecular spectrum of α-thalassemia in the Iranian population of Hormozgan: three novel point mutation defects. Am J Hematol. 2003;74(2):99–103.
- Yap ZM, Sun KM, Teo CR, et al. Evidence of differential selection for the -α(3.7) and -α(4.2) single-α-globin gene deletions within the same population. Eur J Haematol. 2013;90(3):210–213.
- Abbasi-Moheb L, Poorfathollah AA, Kahrizi K, et al. α-Thalassemia: deletion analysis in Iran. Arch Iran Med. 2001;4(4):160–164.
- Sarookhani MR, Asiabanha M. Spectrum of α-thalassemia mutations in Qazvin Province Iran. Afr J Biotechnol. 2011;10(77):17690–17694.
- Hadavi V, Taromchi AH, Malekpour M, et al. Elucidating the spectrum of α-thalassemia mutations in Iran. Haematologica. 2007;92(7):992–993.
- Hellani A, Fadel E, El-Sadadi S, et al. Molecular spectrum of α-thalassemia mutations in microcytic hypochromic anemia patients from Saudi Arabia. Genet Test Mol Biomarkers. 2009;13(2):219–221.
- Kanavakis E, Papassotiriou I, Karagiorga M, et al. Phenotypic and molecular diversity of Haemoglobin H disease: a Greek experience. Br J Haematol. 2000;111(3):915–923.
- Baysal E. α-Thalassemia syndromes in the United Arab Emirates. Hemoglobin. 2011;35(5-6):574–580.
- Hadavi V, Jafroodi M, Hafezi-Nejad N, et al. α-Thalassemia mutations in Gilan Province, North Iran. Hemoglobin. 2009;33(3):235–241.
- Jassim N, Al-Arrayed S, Gerard N, et al. Molecular basis of α-thalassemia in Bahrain. Bahrain Med Bull. 2001;23(1):3–7.
- Dehbozorgian J, Moghadam M, Daryanoush S, et al. Distribution of α-thalassemia mutations in Iranian population. Hematology. 2015;20(6):359–362.
- Harteveld CL, Higgs DR. α-Thalassaemia. Orphanet J Rare Dis. 2010;5:13. doi: 10.1186/1750-1172-5-13.