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Hemoglobin
international journal for hemoglobin research
Volume 36, 2012 - Issue 1
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Original Article

Hb H Disease with Various β Hemoglobinopathies: Molecular, Hematological and Diagnostic Aspects

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Pages 18-24 | Received 05 Jun 2011, Accepted 30 Jun 2011, Published online: 06 Dec 2011

REFERENCES

  • Chui DHK, Fucharoen S, Chan V. Hemoglobin H disease: not necessarily a benign disorder. Blood. 2003;101(3):791–800.
  • Fucharoen S, Winichagoon P, Sirithanaratkul N, Chawthaworn J, Pootrakul P. α- And β-thalassemia in Thailand. Ann NY Acad Sci. 1998;850:412–414.
  • Fucharoen S, Ayukarn K, Sanchaisuriya K, Fucharoen G. A typical Hemoglobin H disease in a Thai patient resulting from a combination of α-thalassemia 1 and Hemoglobin Constant Spring with Hemoglobin J Bangkok heterozygosity. Eur J Haematol. 2001;66(5):312–316.
  • Jetsrisuparb A, Sanchaisuriya K, Fucharoen G, Fucharoen S, Wiangnon S, Komwilaisak P. Triple heterozygosity of a hemoglobin variant: Hemoglobin Pyrgos with other hemoglobinopathies. Int J Hematol. 2002;75(1):35–39.
  • Yamsri S, Sanchaisuriya K, Fucharoen G, Sae-ung N, Fucharoen S. Genotype and phenotype characterizations in a large cohort of β-thalassemia heterozygote with different forms of α-thalassemia in northeast Thailand. Blood Cells Mol Dis. 2011;47(2)120–124.
  • Fucharoen G, Sanchaisuriya K, Sae-ung N, Dangwibul S, Fucharoen S. A simplified screening strategy for thalassaemia and Haemoglobin E in rural communities in south-east Asia. Bull World Health Organ. 2004;82(5):364–372.
  • Yamsri S, Sanchaisuriya K, Fucharoen G, Sae-ung N, Ratanasiri T, Fucharoen S. Prevention of severe thalassemia in northeast Thailand: 16 years of experience at a single university center. Prenat Diagn. 2010;30(6):540–546.
  • Sanchaisuriya K, Chunpanich S, Fucharoen G, Fucharoen S. Multiplex allele-specific PCR assay for differential diagnosis of Hb S, Hb D-Punjab and Hb Tak. Clin Chim Acta. 2004;343(1–2):129–134.
  • Chunpanich S, Fucharoen S, Sanchaisuriya K, Fucharoen G, Kam-itsara K. Molecular and hematological characterization of Hemoglobin Hope/Hemoglobin E and Hemoglobin Hope/α-thalassemia 2 in Thai patients. Lab Hematol. 2004;10(4): 215–220.
  • Huang Y, Lin M, Wu J-R, Yang L-Y, Xiang Z. Hb CS-H disease combined with β-thalassemia-a case report. Blood Cells Mol Dis. 2009;44(4):215–216.

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