References
- Harteveld CL, Higgs DR. α-Thalassaemia. Orphanet J Rare Dis. 2010;5:13.
- Higgs DR. The molecular basis of α-thalassemia. Cold Spring Harb Perspect Med. 2013;3:a011718.
- De-la-Cruz-Salcedo EI, Ibarra B, Rizo-de-la-Torre LC, et al. Molecular analysis of complex cases of α- and β-thalassemia in Mexican Mestizo patients with microcytosis and hypochromia reveals two novel α0-thalassemia deletions – –Mex1 and – –Mex2. Int J Lab Hematol. 2016;38(5):535–542.
- Huisman THJ, Jonxis JHP. The Hemoglobinopathies Techniques of Identification. New York, NY, USA: 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.
- Liu YT, Old JM, Miles K, et al. Rapid detection of α-thalassaemia deletions and α-globin gene triplication by multiplex polymerase chain reactions. Br J Haematol. 2000;108(2):295–299.
- Ralser M, Querfurth R, Warnatz HJ, et al. An efficient and economic enhancer mix for PCR. Biochem Biophys Res Commun. 2006;347(3):747–751.
- Smit AFA, Hubley R, Green P. RepeatMasker open-4.0.6 [Internet]. Seattle, WA, USA: Institute for Systems Biology. [cited 2016]. Available from: http://www.repeatmasker.org.
- Rosenbloom KR, Armstrong J, Barber GP, et al. The UCSC Genome Browser database: 2015 update. Nucleic Acids Res. 2015;43(D1):D670–D681.
- Eng B, Patterson M, Borys S, et al. PCR-based diagnosis of the Filipino (– –FIL) and Thai (– –THAI) α-Thalassemia-1 deletions. Am J Hematol. 2000;63(1):54–56.
- Sarkar AA, Banerjee S, Chandra S, et al. A novel 33·3 kb deletion (– –KOL) in the α-globin gene cluster: a brief report on deletional α-thalassaemia in the heterogeneous eastern Indian population. Br J Haematol. 2005;130(3):454–457.
- Rüdiger NS, Gregersen N, Kielland-Brandt MC. One short well conserved region of Alu-sequences is involved in human gene rearrangements and has homology with prokaryotic chi. Nucleic Acids Res. 1995;23(2):256–260.
- Harteveld KL, Losekoot M, Fodde R, et al. The involvement of Alu repeats in recombination events at the α-globin gene cluster: characterization of two α0-thalassemia deletion breakpoints. Hum Genet. 1997;99(4):528–534.
- Vanin EF, Henthorn PS, Kioussis D, et al. Unexpected relationships between four large deletions in the human β-globin gene cluster. Cell. 1983;35(3 Pt 2):701–709.
- Nicholls RD, Fischel-Ghodsian N, Higgs DR. Recombination at the human α-globin gene cluster: sequence features and topological constraints. Cell. 1987;49(3):369–378.
- Rugless MJ, Fisher CA, Old JM, et al. A large deletion in the human α-globin cluster caused by a replication error is associated with an unexpectedly mild phenotype. Hum Mol Genet. 2008;17(19):3084–3093.