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Hemoglobin
international journal for hemoglobin research
Volume 40, 2016 - Issue 3
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Original Article

Identification of the −α2.4 Deletion in One Family and in One Hb H Disease Patient in Guangxi, People’s Republic of China

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Pages 194-197 | Received 20 Nov 2015, Accepted 02 Feb 2016, Published online: 17 Mar 2016

References

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  • Higgs DR, Engel JD, Stamatoyannopoulos G. Thalassaemia. Lancet. 2012;379(9813):373–383
  • Zhao JB, Zhao L, Fei YJ, et al. A novel α thalassemia 2 (−2.7 kb) observed in a Chinese patient with Hb H disease. Am J Hematol. 1991;38(3):248–249
  • Eng B, Walsh R, Walker L, et al. Characterization of a rare single α-globin gene deletion in a Chinese woman with Hb H disease. Hemoglobin. 2005;29(4):297–299
  • Lin M, Wu JR, Huang Y, et al. Clinical and molecular characterization of a rare 2.4 kb deletion causing α+ thalassemia in a Chinese family. Blood Cells Mol Dis. 2012;49(2):83–84
  • So CC, Chan AYY, Ma ESK. Novel point mutation of the α2-globin gene (HBA2) and a rare 2.4 kb deletion of the α1-globin gene (HBA1), identified in two Chinese patients with Hb H disease. Hemoglobin. 2014;38(3):213–215
  • Long J, Yan S, Lao K, et al. The diagnosis and molecular analysis of a novel 21.9 kb deletion (Qinzhou type deletion) causing α+ thalassemia. Blood Cells Mol Dis. 2014;52(4):225–229
  • Long J, Pang W, Sun L, et al. Diagnosis of a family with the novel −α21.9 thalassemia deletion. Hemoglobin. 2015;39(6):419–422

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