REFERENCES
- Hardison RC, Chui DHK, Giardine B, et al. HbVar: a relational database of human hemoglobin variants and thalassemia mutations at the globin gene server. Hum Mutat. 2002;19(3):225–233 (http://globin.cse.psu.edu).
- Patrinos GP, Giardine B, Riemer C, et al. Improvements in the HbVar human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res. 2004;32(Database issue):D537-D541 (http://globin.cse.psu.edu).
- Li D, Liao C, Li J, Prenatal diagnosis of β-thalassemia by reverse dot-blot hybridization in Southern China. Hemoglobin. 2006;30(3):365–370.
- Chong SS, Boehm CD, Higgs DR, Cutting GR. Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia. Blood. 2000;95(1):360–362.
- Chan V, Yam I, Chen FE, Chan TK. A reverse dot-blot method for rapid detection of non-deletion α thalassaemia. Br J Haematol. 1999;104(3):513–515.
- Ko TM, Tseng LH, Hsu PM, Molecular characterization of β-thalassemia in Taiwan and the identification of two new mutations. Hemoglobin. 1997;21(2):131–142.
- Rund D, Cohen T, Filon D, Evolution 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.
- Indrak K, Indrakova J, Kutlar F, Compound heterozygosity for a β0-thalassemia (frameshift codons 38/39; –C) and a nondeletional Swiss type of HPFH (A→C at nt –110, Gγ) in a Czechoslovakian family. Ann Hematol. 1991;63(2):111–115.
- Fucharoen S, Fucharoen G, Laosombat V, Fukumaki Y. Double heterozygosity of the β-Malay and a novel β-thalassemia gene in a Thai patient. Am J Hematol 1991; 38(2):142–144.
- Ringelhann B, Szelenyi JG, Horanyi M, Molecular characterization of β-thalassemia in Hungary. Hum Genet. 1993;92(4):385–387.
- Landin B, Berglund S. A novel mutation in the β-globin gene causing β-thalassaemia in a Swedish family. Eur J Haematol. 1996;57(2):182–184.