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Hemoglobin
international journal for hemoglobin research
Volume 32, 2008 - Issue 3
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Original

Molecular Basis of α-Thalassemia in Algeria

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Pages 273-278 | Received 27 Mar 2007, Accepted 05 Jul 2007, Published online: 07 Jul 2009

REFERENCES

  • Trabuchet G, Belhani M, Richard F, Hamladji RM, Benabadji M, Colonna P. Premières observations d'alpha thalassemie en Algérie: 12 cas d'hémoglobinose H. Sem Hôp Paris 1977; 53(16)885–889
  • Henni T, Bachir D, Tabone P, Jurdic P, Godet J, Colonna P. Hemoglobin Bart's in Northern Algeria. Acta Haematologica 1981; 65(4)240–246
  • Henni T, Morlé F, Lopez B, Colonna P, Godet J. α-Thalassemia haplotypes in the Algerian population. Hum Genet 1987; 75(3)272–276
  • Leclerc T, Guetarni D, Bernet A, Colonna P, Godet J, Morlé F. Identification of three different α-thalassemic haplotypes: −α3.7, (– –)MED, αHph Iα in the same Algerian family. Hum Mutat 1995; 5(2)182–183
  • Kattamis C, Camaschella C, Sivera P, Surrey S, Fortina P. Human α-thalassemia syndromes: detection of molecular defects. Am J Hematol 1996; 53(2)81–91
  • Baysal E, Huisman THJ. Detection of common deletional α-thalassemia-2 determinants by PCR. Am J Hematol 1994; 46(3)208–213
  • Bowden DK, Vickers MA, Higgs DR. A PCR-based strategy to detect the common severe determinants of α thalassaemia. Br J Haematol 1992; 81(1)104–118
  • Treager-Synodinos J, Kanavakis E, Tsezis M, Kattamis A, Kattamis C. Characterization of nondeletional α thalassemia mutations in the Greek population. Am J Hematol 1993; 44(3)162–167
  • Jassim N, AL-Arrayed S, Gerard N, Al-Mukharraq H, Al-Ajami A, Ramasawmy R, Krishnamoorthy R. A mismatched-primer polymerase chain reaction-restriction fragment length polymorphism strategy for rapid screening of the polyadenylation signal mutation αT-Saudi (AATAAA→AATAAG) in the α2-globin gene. Hemoglobin 1999; 23(3)213–220
  • Mirabile E, Samperi P, Di Catalo A, Poli A, La Spina M, Schiliro G. Phenotype-genotype correlation in Sicilian patients with Hb H. J Eur Haematol 2000; 65(5)306–309
  • Peres MJ, Romão L, Carreiro H, Picanço I, Batalha L, Magalhães HA, Martins MC, Lavinha J. Molecular basis of α-thalassemia in Portugal. Hemoglobin 1995; 19(6)343–352
  • Pirastu M, Lee KY, Dozy AM, Kan YW, Stamatoyannopoulos G, Hadjiminas MG, Zachariades Z, Angius A, Furbetta M, Rosatelli C, Cao A. α-Thalassemia in two Mediterranean populations. Blood 1982; 60(2)509–512
  • Harteveld KL, Heister AJGAM, Giordano PC, Losekoot M, Bernini LF. Rapid detection of point mutations and polymorphisms of the α-globin genes by DGGE and SSCA. Hum Mutat 1996; 7(2)114–122
  • Zorai A, Harteveld CL, Bakir A, van Delft P, Falfoul A, Dellagi K, Abbes S, Giordano PC. Molecular spectrum of α-thalassemia in Tunisia: epidemiology and detection at birth. Hemoglobin 2002; 26(4)353–362
  • Bachir D, Belhani M, Godet J, Nigon V, Colonna P. Indirect evaluation of a gene frequency: calculation of β-thalassemia frequency in Algeria based on associated hemoglobin variants frequency. Hum Hered 1984; 34(3)187–191
  • Higgs DR, Vickers MA, Wilkie AOM, Pretorius I-M, Jarman AP, Weatherall DJ. A review of the molecular genetics of the human α-globin gene cluster. Blood 1989; 73(5)1081–1104
  • Fichera M, Spalletta A, Fiorenza F, Lombardo T, Schiliro G, Tamouza R, Lapoumeroulie C, Labie D, Ragusa A. Molecular basis of α-thalassemia in Sicily. Hum Genet 1997; 99(3)381–386
  • Zorai A, Abbes S, Préhu C, Omar S, Gerard N, Hafsia R, Asma B, Guemira F, Dellagi K. Hb H disease among Tunisians: molecular characterization of α-thalassemia determinants and hematological findings. Hemoglobin 2003; 27(1)57–61
  • Pressley L, Higgs DR, Clegg JB, Perrine RP, Pembrey ME, Weatherall DJ. A new genetic basis for Hemoglobin H disease. N Engl J Med 1980; 303(24)1383–1388
  • Thein SL, Wallace RB, Pressley L, Clegg JB, Weathrall DJ, Higgs DR. The polyadenylation site mutation in the α-globin gene cluster. Blood 1988; 71(2)313–319
  • Bernini LF. Geographic distribution of α-thalassemia. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management, MH Steinberg. Cambridge University Press, Cambridge 2001; 878–894
  • Labie D, Benabadji M, Elion J. Genetic disorders in North African populations of the Maghreb. Genetic Disorders Among Arab Populations, AS Teebi, TI Farag. Oxford University Press, New York 1997; 290–321

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