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Hemoglobin
international journal for hemoglobin research
Volume 32, 2008 - Issue 5
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Short Communications

Association of β-Thalassemia and Hb Q-Thailand Resulting in a Normal Hb A2 Value

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Pages 505-508 | Received 11 Jun 2007, Accepted 10 Oct 2007, Published online: 07 Jul 2009

REFERENCES

  • Li D, Liao C, Li J, Huang Y, Xie X, Wei J, Wu S. Prenatal diagnosis of β-thalassemia by reverse dot-blot hybridization in southern China. Hemoglobin 2006; 30(3)365–370
  • Pirastu M, Ristaldi MS, Loudianos G, Murru S, Sciarratta GV, Parodi MI, Leone D, Agosti S, Cao A. Molecular analysis of atypical β-thalassemia heterozygotes. Ann NY Acad Sci 1990; 612: 90–97
  • Eram SM, Azimifar B, Abolghasemi H, Foulady P, Lotfi V, Masrouri M, Hosseini M, Abdolhosseini A, Zeinali S. The IVS-II-1 (G→A) β0-thalassemia mutation in cis with Hb A2-Troodos [δ116(G18)Arg→Cys (CGC→TGC)] causes a complex prenatal diagnosis in an Iranian family. Hemoglobin 2005; 29(4)289–292
  • Zeng FY, Fucharoen S, Huang SZ, Rodgers GP. Hb Q-Thailand [α74(EF3)Asp→His]: gene organization, molecular structure, and DNA diagnosis. Hemoglobin 1992; 16(6)481–491

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