REFERENCES
- Olivieri NF. The β-thalassemias. N Engl J Med. 1999; 341(2)99–109
- Clark BE, Thein SL. Molecular diagnosis of haemoglobin disorders. Clin Lab Haematol. 2004; 26(3)159–176
- Lemsaddek W, Picanco I, Seuanes F, Nogueira P, Mahmal L, Benchekroun S, et al. The β-thalassemia mutation/haplotype distribution in the Moroccan population. Hemoglobin. 2004; 28(1)25–37
- Agouti I, Badens C, Abouyoub A, Levy N, Bennani M. Molecular basis of β-thalassemia in Morocco: possible origins of the molecular heterogeneity. Genet Test. 2008; 12(4)563–568
- Agouti I, Bennani M, Abouyoub A, Barakat A, Khattab M, Badens C. Thalassemia intermedia due to a novel mutation in the second intervening sequence of the β-globin gene. Hemoglobin. 2007; 31(4)433–438
- Agouti I, Bennani M, Nezri M, Levy N, Badens C. β-Thalassemia intermedia due to two novel mutations in the promoter region of the β-globin gene. Eur J Haematol. 2008; 80(4)346–350
- 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
- Shaji RV, Chandy SM, Krishnamoorthy R. A single tube multiplex PCR method to detect the common β+ thalassemia alleles. Blood. 2000; 95(5)1879–1880
- Dode C, Krishnamoorthy R, Lamb J, Rochette J. Rapid analysis of –α3.7 thalassaemia and αααanti 3.7 triplication by enzymatic amplification analysis. Br J Haematol. 1993; 83(1)105–111
- Antonarakis SE, Kazazian HH, Jr, Orkin SH. DNA polymorphism and molecular pathology of the human globin gene clusters. Hum Genet. 1985; 69(1)1–14
- Goldsmith ME, Humphries RK, Ley T, Cline A, Kantor JA. Nienhuis AW. ‘Silent’ nucleotide substitution in a β+-thalassemia globin gene activates splice site in coding sequence RNA. Proc Natl Acad Sci USA. 1983; 80(8)2318–2322
- Gonzalez-Redondo JM, Kutlar A, Kutlar F, McKie VC, McKie KM, Baysal E, et al. Molecular characterization of Hb S(C) β-thalassemia in American Blacks. Am J Hematol. 1991; 38(1)9–14
- Bennani C, Bouhass R, Perrin-Pecontal P, Tamouza R, Malou M, Elion J, et al. Anthropological approach to the heterogeneity of β-thalassemia mutations in northern Africa. Hum Biol. 1994; 66(3)369–382
- Chehab FF, Der Kaloustian V, Khouri FP, Deeb SS, Kan YW. The molecular basis of β-thalassemia in Lebanon: application to prenatal diagnosis. Blood. 1987; 69(4)1141–1145
- Nozari G, Rahbar S. Golshaiyzan A, Rahmanzadeh S. Molecular analyses of β-thalassemia in Iran. Hemoglobin. 1995; 19(6)425–431
- Filon D, Oron V, Krichevski S, Shaag A, Shaag Y, Warren TC, et al. Diversity of β-globin mutations in Israeli ethnic groups reflects recent historic events. Am J Hum Genet. 1994; 54(5)836–843
- Kantor JA, Turner PH, Nienhuis AW. β-Thalassemia: Mutations which affect processing of the β-globin mRNA precursor. Cell. 1980; 21(1)149–157
- Gonzalez-Redondo JM, Stoming TA, Lanclos KD, Gu YC, Kutlar A, Kutlar F, et al. Clinical and genetic heterogeneity in Black patient with homozygous β-thalassemia from the Southeastern United States. Blood. 1988; 72(3)1007–1014
- Hattori Y, Yamane A, Yamashiro Y, Matsuno Y, Yamamoto K, Yamamoto K, et al. Characterization of β-thalassemia mutations among Japanese. Hemoglobin. 1989; 13(7)657–670
- Orkin SH, Kazazian HH, Jr., Antonarakis SE, Goff SC, Boehm CD, Sexton JP, et al. Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster. Nature. 1982; 296(5858)627–631