Profile of β-Thalassemia and its Prenatal Diagnosis in Khorasan-E-Jonobi Province, Iran

REFERENCES

• Weatherall DJ, Clegg JB, Eds. The Thalassaemia Syndromes, 4th ed. Oxford: Blackwell Science, 2001.
   Google Scholar
• Cao A, Rosatelli MC, Monni G, Galanello R. Screening for thalassemia: a model of success. Obstet Gynecol Clin North Am. 2002;29(2):305–328, vi-vii.
   PubMed Web of Science ®Google Scholar
• Rahimi Z, Muniz A, Parsian A. Detection of responsible mutations for β-thalassemia in the Kermanshah Province of Iran using PCR-based techniques. Mol Biol Rep. 2010;37(1):149–154.
   PubMed Web of Science ®Google Scholar
• Cao A, Galanello R. β-Thalassemia. Genet Med. 2010;12(2):61–76.
   PubMed Web of Science ®Google Scholar
• Haghi M, Khorshidi S, Hosseinpour Feizi MA, Pouladi N, Hosseinpour Feizi AA. β-Thalassemia mutations in the Iranian Kurdish population of Kurdistan and West Azerbaijan provinces. Hemoglobin. 2009;33(2):109–114.
   PubMed Web of Science ®Google Scholar
• Nikuei P, Hadavi V, Rajaei M, Saberi M, Hajizade F, Najmabadi H. Prenatal diagnosis for β-thalassemia major in the Iranian Province of Hormozgan. Hemoglobin. 2008;32(6):539–545.
   PubMed Web of Science ®Google Scholar
• Zadeh-Vakili A, Eshghi P. Detection of a rare mutation in an Iranian family: codons 37/38/39 (7 bp deletion). Hemoglobin. 2009;33(6):523–527.
   PubMed Web of Science ®Google Scholar
• Derakhshandeh-Peykar P, Akhavan-Niaki H, Tamaddoni A, . Distribution of β-thalassemia mutations in the northern provinces of Iran. Hemoglobin. 2007;31(3):351–356.
   PubMed Web of Science ®Google Scholar
• Najmabadi H, Ghamari A, Sahebjam F, . Fourteen-year experience of prenatal diagnosis of thalassemia in Iran. Community Genet. 2006;9(2):93–97.
   PubMedGoogle Scholar
• Najmabadi H, Karimi-Nejad R, Sahebjam S, . The β-thalassemia mutation spectrum in the Iranian population. Hemoglobin. 2001;25(3):285–296.
   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, . 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
• Merat A, Haghshenas M, Pour ZM, . β-Thalassemia in southwestern Iran. Hemoglobin. 1993;17(5):427–437.
   PubMed Web of Science ®Google Scholar
• Miri-Moghaddam E, Zadeh-Vakili A, Rouhani Z, Naderi M, Eshghi P, Khazaei Feizabad A. Molecular basis and prenatal diagnosis of β-thalassemia among Balouch population in Iran. Prenat Diagn. 2011;31(8):788–791.
   PubMed Web of Science ®Google Scholar
• Hosseinpour Feizi MA, Hosseinpour Feizi AA, Pouladi N, Haghi M, Azarfam P. Molecular spectrum of β-thalassemia mutations in Northwestern Iran. Hemoglobin. 2008;32(3):255–261.
   PubMed Web of Science ®Google Scholar
• Newton CR, Graham A, Heptinstall LE, . Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS). Nucleic Acids Res. 1989;17(7):2503–2516.
   PubMed Web of Science ®Google Scholar
• Old JM. Screening and genetic diagnosis of haemoglobin disorders. Blood Rev. 2003;17(1):43–53.
   PubMed Web of Science ®Google Scholar
• Liu YT, Old JM, Miles K, Fisher CA, Weatherall DJ, Clegg JB. Rapid detection of α-thalassaemia deletions and α-globin gene triplication by multiplex polymerase chain reactions. Br J Haematol. 2000;108(2):295–299.
   PubMed Web of Science ®Google Scholar
• Sutcharitchan P, Wang W, Settapiboon R, Amornsiriwat S, Tan AS, Chong SS. Hemoglobin H disease classification by isoelectric focusing: molecular verification of 110 cases from Thailand. Clin Chem. 2005;51(3):641–644.
   PubMed Web of Science ®Google Scholar
• Old JM, Petrou M, Modell B, Weatherall DJ. Feasibility of antenatal diagnosis of β thalassaemia by DNA polymorphisms in Asian Indian and Cypriot populations. Br J Haematol 1984;57(2):255–263.
   PubMed Web of Science ®Google Scholar
• Ghotbi N, Tsukatani T. Evaluation of national health policy of thalassemia screening in the Islamic Republic of Iran. East Mediterr Health J. 2005;11(3):308–318.
   PubMedGoogle Scholar
• Akbari MT, Izadi P, Izadyar M, Kyriacou K, Kleanthous M. Molecular basis of thalassemia intermedia in Iran. Hemoglobin. 2008;32(5):462–470.
   PubMed Web of Science ®Google Scholar
• Kiani AA, Mortazavi Y, Zeinali S, Shirkhani Y. The molecular analysis of β-thalassemia mutations in Lorestan Province, Iran. Hemoglobin. 2007;31(3):343–349.
   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
• 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
• Saleh-Gohari N, Bazrafshani M. Distribution of β-globin gene mutations in thalassemia minor population of Kerman Province, Iran. Iranian J Publ Health. 2010;39(2):69–76.
   PubMed Web of Science ®Google Scholar
• Treisman R, Orkin SH, Maniatis T. Specific transcription and RNA splicing defects in five cloned β-thalassemia genes. Nature. 1983;302(5909):591.
   PubMed Web of Science ®Google Scholar
• Ahmed S, Petrou M, Saleem M. Molecular genetics of β-thalassaemia in Pakistan: a basis for prenatal diagnosis. Br J Haematol. 1996;94(3):476–482.
   PubMed Web of Science ®Google Scholar
• Tadmouri GO, Gulen RI. Deniz: the electronic database for β-thalassemia mutations in the Arab world. Saudi Med J. 2003;24(11):1192–1198.
   PubMed Web of Science ®Google Scholar
• Lahiry P, Al-Attar SA, Hegele RA. Understanding β-thalassemia with focus on the Indian Subcontinent and the Middle East. Open Hematol J. 2008;2:5–13.
   Google Scholar
• Derakhshandeh-Peykar P, Hourfar H, Heidari M, Kheirollahi M, Miryounesi M. The spectrum of β-thalassemia mutations in Isfahan Province of Iran. Iranian J Publ Health. 2008;37(2):106–111.
   Web of Science ®Google Scholar
• Sarookhani MR, Ahmadi MH, Amirizadeh N. Molecular spectrum of β-globin mutations in transfusion-dependent patients with thalassemia in Qazvin Province, Iran. Iranian J Med Sci. 2008;34(1):17–22.
   Google Scholar
• Rahimi Z, Muniz A, Parsian A. Detection of responsible mutations for β thalassemia in the Kermanshah Province of Iran using PCR-based techniques. Mol Biol Rep. 2010;37(1):149–154.
   PubMed Web of Science ®Google Scholar
• Schnee J, Griese E-U, Eigel A, Horst J. β-Thalassemia gene analysis in Turkish family reveals a 7 bp deletion in coding region. Blood. 1989;73(8):2224–2225.
   PubMed Web of Science ®Google Scholar