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Hemoglobin
international journal for hemoglobin research
Volume 36, 2012 - Issue 2
131
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Short Communications

Association of Hb New York with Hb E and α0-Thalassemia in a Chinese Woman Identified by Sebia Capillarys2 System

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Pages 157-160 | Received 30 Oct 2011, Accepted 02 Dec 2011, Published online: 22 Feb 2012

REFERENCES

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  • Orkin SH, Kazazian HH Jr, Antonarakis SE, Ostrer H, Goff SC, Sexton JP. Abnormal RNA processing due to the exon mutation of βE-globin gene. Nature. 1982;300(5894):768–769.
  • Lee AC, Ma ES, Chan AY, Szeto SC, Chan LC. Double heterozygosity for Hb New York [β113 GTG>GAG; Val→Glu] and β0-thalassemia mutations manifests as a thalassemia trait. Pediatr Hematol Oncol. 2008; 25(3):227–231.
  • Li D, Liao C, Li J, Xie X, Huang Y, Zhong H. Detection of α-thalassemia in β-thalassemia carriers and prevention of Hb Bart’s hydrops fetalis through prenatal screening. Haematologica. 2006;91(5):649–651.

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