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Hemoglobin
international journal for hemoglobin research
Volume 36, 2012 - Issue 4
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Short Communication

Hb J-Wenchang-Wuming [α11(A9)Lys→Gln (AAG>CAG) (α2 or α1)] Compromises Neonatal Screening for α-Thalassemia with the Sebia Capillarys2 Electrophoresis System

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Pages 395-398 | Received 02 Feb 2012, Accepted 12 Mar 2012, Published online: 08 Jun 2012

REFERENCES

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  • Kemper AR, Knapp AA, Metterville DR, Comeau AM, Green NS, Perrin JM. Weighing the evidence for newborn screening for Hemoglobin H disease. J Pediatr. 2011;158(5):780–783.
  • Kyriacou K, Kyrri A, Kalogirou E, Hb Bart’s levels in cord blood and α-thalassemia mutations in Cyprus. Hemoglobin 2000;24(3):171–180.
  • Rugless MJ, Fisher CA, Stephens AD, Amos RJ, Mohammed T, Old JM. Hb Bart’s in cord blood: an accurate indicator of α-thalassemia. Hemoglobin. 2006;30(1):57–62.
  • Lin TM, Eng HL, Kuo PL, Wu HL. Neonatal screening for α -thalassemia in southern Taiwan. J Formos Med Assoc. 1992;91(12):1213–1215.
  • Munkongdee T, Pichanun D, Butthep P, Quantitative analysis of Hb Bart’s in cord blood by capillary electrophoresis system. Ann Hematol. 2011;90(7):741–746.

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