The Molecular Analysis of β-Thalassemia Mutations in Lorestan Province, Iran

REFERENCES

• Mahboudi F, Zeinali S, Merat A, Delmaghani S, Mostafavipour K, Moghaddam Z, Haghshenas M. The molecular basis of β thalassemia mutation in Fars province, Iran. Irn J Med Sci 1996; 21(3&4)104–6
   Google Scholar
• Samavat A, Modell B. Iranian national thalassaemia screening programme. BMJ 2004; 329(7475)1134–1137
   PubMed Web of Science ®Google Scholar
• Najmabadi H, Karimi-Nejad R, Sahebjam S, Pourfarzad F, Teimourian S, Sahebjam F, Amirizadeh N, Karimi-Nejad MH. The β-thalassemia mutation spectrum in the Iranian population. Hemoglobin 2001; 25(3)285–296
   PubMed Web of Science ®Google Scholar
• Merat A, Haghshenas M, Mostafavi Pour Z, Plonczynski MW, Harrell AN, Coleman MB, Steinberg MH. β-Thalassemia in southwestern Iran. Hemoglobin 1993; 17(5)427–437
   PubMed Web of Science ®Google Scholar
• Najmabadi H, Pourfathollah AA, Neishabury M, Sahebjam F, Krugluger W, Oberkanins C. Rare and unexpected mutations among Iranian β-thalassemia patients and prenatal samples discovered by reverse-hybridization and DNA sequencing. Haematologica 2002; 87(10)1113–1114
   PubMed Web of Science ®Google Scholar
• Karimi M, Karamifar HA. Short stature in β-thalassemia minor subjects. Med Sci Monit 2004; 10(11)CR603–CR605
   PubMed Web of Science ®Google Scholar
• Yavarian M, Harteveld CL, Batelaan D, Bernini LF, Giordano PC. Molecular spectrum of β-thalassemia in the Iranian Province of Hormozgan. Hemoglobin 2001; 25(1)35–43
   PubMed Web of Science ®Google Scholar
• Noori-Daloii MR, Moazami N, Farhangi S, Atalay A, Geren IN, Akar L, Atalay EO, Çirakoglu B, Bermek E. β-Thalassemia in Iran: a high incidence of the nonsense codon 39 mutation on the island of Queshm. Hemoglobin 1994; 18(6)449–453
   PubMed Web of Science ®Google Scholar
• Karimi M, Yarmohammadi H, Farjadian S, Zeinali S, Moghaddam Z, Cappellini MD, Giordano PC. β-Thalassemia intermedia from southern Iran: IVS-II-1 (G→A) is the prevalent thalassemia intermedia allele. Hemoglobin 2002; 26(2)147–154
   PubMed Web of Science ®Google Scholar
• Goossens M, Kan YW. DNA analysis in the diagnosis of hemoglobin disorders. Methods Enzymol 1981; 76: 805–817
   PubMedGoogle Scholar
• Old J, Varawalla N, Weatherall D. Rapid detection and prenatal diagnosis of β thalassaemia: studies in Indian and Cypriot populations in the UK. Lancet 1990; 336(8719)834–837
   PubMed Web of Science ®Google Scholar
• Dilmaghani S, Zeinali S, Moghaddam ZK, Golbari R, Sarhaddi M, Akhoondzahed M. Abstract 28. Proceedings of the 6th International Conference on Thalassaemia and the Haemoglobinopathies. 1997
   Google Scholar
• Dilmaghani S, Zeinali S, Moghaddam ZK, Sarhadi M, Golbari R, Akhoondzahed A, Sanei E. Abstract 29. Proceedings of the 6th International Conference on Thalassaemia and the Haemoglobinopathies, Malta, April, 1997
   Google Scholar
• Khodaie H, Zeinali S, Dilmaghani S, Moghadam ZK, Sarhadi M, Golbari R, Mojoudi AR. Abstract 30. Proceedings of the 6th International Conference on Thalassaemia and the Haemoglobinopathies. 1997
   Google Scholar
• Nozari G, Rahbar S, Golshaiyzan A, Rahmanzadeh S. Molecular analyses of β-thalassemia in Iran. Hemoglobin 1995; 19(6)425–431
   PubMed Web of Science ®Google Scholar
• Zeinali S, Moghaddam ZK, Dilmaghani S, Sarhaddi M, Golbari R, Akhoondezahed A, Ghadiri M, Khaladj V. Abstract 31. Proceedings of the 6th International Conference on Thalassaemia and the Haemoglobinopathies. 1997
   Google Scholar
• El-Latif MA, Filon D, Rund D, Oppenheim A, Kanaan M. The β+-IVS-I-6 (T→C) mutation accounts for half of the thalassemia chromosomes in the Palestinian populations of the mountain regions. Hemoglobin 2002; 26(1)33–40
   PubMed Web of Science ®Google Scholar
• Tadmouri GO, Tuzmen S, Basak AN. Rare β-thalassemia mutation in a Turkish patient: FSC-36/37 (–T). Hum Biol 1997; 69(2)263–267
   PubMed Web of Science ®Google Scholar
• Adekile AD, Gu L-H, Baysal E, Haider MZ, al-Fuzae L, Aboobacker KC, al-Rashied A, Huisman THJ. Molecular characterization of α-thalassemia determinants, β-thalassemia alleles, and βShaplotypes among Kuwaiti Arabs. Acta Haematol 1994; 92(4)176–181
   PubMed Web of Science ®Google Scholar
• el-Hazmi MAF, Warsy AS, al-Swailem AR. The frequency of 14 β-thalassemia mutations in the Arab populations. Hemoglobin 1995; 19(6)353–360
   PubMed Web of Science ®Google Scholar
• Khan SN, Riazuddin S. Molecular characterization of β-thalassemia in Pakistan. Hemoglobin 1998; 22(4)333–345
   PubMed Web of Science ®Google Scholar
• Colah R, Nadkarni A, Gorakshakar A, Phanasgaonkar S, Surve R, Subramaniam PG. Impact of β globin gene mutations on the clinical phenotype of β thalassemia in India. Blood Cells Mol Dis 2004; 33(2)153–157
   PubMed Web of Science ®Google Scholar
• Atalay EO, Çirakoglu B, Dinçol G, Atalaty A. Regional distribution of β thalassemia mutation in Turkey. Int J Hematol 1993; 57(3)207–211
   PubMed Web of Science ®Google Scholar