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Hemoglobin
international journal for hemoglobin research
Volume 33, 2009 - Issue 3-4
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Original Article

A Novel Deletional β-Thalassemic Variant in an Ethnic Qatari Patient

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Pages 214-219 | Received 14 Dec 2008, Accepted 15 Feb 2009, Published online: 15 Sep 2009

REFERENCES

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  • Cai SP, Wall J, Kan YW, Chehab FF. Reverse dot blot probes for screening of β-thalassaemia mutations in Asians and American Blacks. Hum Mutat. 1994; 3(1)59–63
  • Baysal E, Huisman THJ. Detection of common deletional α-thalassemia-2 determinants by PCR. Am J Hematol. 1994; 46(3)208–213
  • Orkin SH, Sexton JP, Goff SC, Kazazian HH. Inactivation of an acceptor RNA splice site by a short deletion in β-thalassemia. J Biol Chem. 1983; 258(12)7249–7251
  • Hardison RC, Chui DHK, Giardine B, et al. HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the glonin gene server. Hum Mutat. 2002; 19(3)225–233, http://globin.cse.psu.edu
  • Patrinos GP, Giardine B, Reimer C, et al. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res. 2004; 32(Database issue)D537–D541, http://globin.cse.psu.edu

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