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Hemoglobin
international journal for hemoglobin research
Volume 28, 2004 - Issue 1
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Original Article

A New Hb Evanston Allele [α14(A12)Trp → Arg] Found Solely, and in the Presence of Common α‐Thalassemia Deletions, in Three Independent Asian Cases

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Pages 1-5 | Received 01 Aug 2003, Accepted 03 Sep 2003, Published online: 24 Aug 2009

References

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  • Honig G R, Shamsuddin M, Vida L N, Mompoint M, Valcourt E, Bowie L J, Jones E C, Powers P A, Spritz R A, Guis M, Embury S H, Conboy J, Kan Y W, Mentzer W C, Weil S C, Hirata R K, Waloch J, O'Riordan J F, Goldstick T K. Hemoglobin Evanston (α14 Trp → Arg). An unstable α‐chain variant expressed as α‐thalassemia. J Clin Invest 1984; 73(6)1740–1749
  • Giordano P C, van Delft P, Batelaan D, Harteveld C L, Bernini L F. Hemoglobinopathy analyses in the Netherlands: a report of an in vitro globin chain biosynthesis survey using a rapid, modified method. Clin Lab Haematol 1999; 21(4)247–255
  • Abraham E C, Reese A, Stalling M, Huisman T HJ. Separation of human hemoglobins by DEAE‐cellulose chromatography using glycine–KCN–NaCl developers. Hemoglobin 1976–1977; 1(1)27–44
  • Harteveld C L, Losekoot M, Haak H, Heister J GAM, Giordano P C, Bernini L F. A novel polyadenylation signal mutation in the α2‐globin gene causing thalassaemia. Br J Haematol 1994; 87(1)139–143

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