References
- Harteveld C L, Wijermans P W, de Ree J ELM, Ter Hal P, Van Delft P, Van Rooijen‐Nijdam I H, Rasp E, Kok P JMJ, Souverijn J HM, Versteegh F GH, Giordano P C. 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. Hemoglobin 2004; 28(1)1–5
- 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
- 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 thalassemia. Br J Haematol 1994; 87(1)139–143
- Harteveld C L, Yavarian M, Zorai A, Quakkelaar E D, Van Delft E D, Giordano P C. The molecular spectrum of α‐thalassemia in the Iranian Population of Hormozgan: three novel mutation defects. Am J Hematol 2003; 74(2)99–103
- Liu Y T, Old J M, Miles K, Fisher C A, Weatherall D J, Clegg J B. Rapid detection of α‐thalassaemia deletions and α‐globin gene triplications by multiplex polymerase chain reaction. Br J Haematol 2000; 108(2)295–299
- Chong S S, Boehm C D, Higgs D R, Cutting G R. Single tube multiplex‐PCR screen for common deletional determinants of α‐thalassemia. Blood 2000; 95(1)360–362
- Sanguansermsri T, Matragoon S, Changloah L, Flatz G. Hemoglobin Suan‐Dok (α2 109 (G16) Leu→Argβ2): an unstable variant associated with α‐thalassemia. Hemoglobin 1979; 3(2&3)161–174
- Hundrieser J, Sanguansermsri T, Laig M, Pape M, Kuhnau W, Flatz G. Direct demonstration of the Hb Suan‐Dok mutation in the α2‐globin gene by restriction analysis with Sma I. Hemoglobin 1990; 14(1)69–77
- Weiss I, Cash F E, Coleman M B, Pressley A, Adams J G, Sanguansermsri T, Liebhaber S A, Steinberg M H. Molecular basis for α‐thalassemia associated with the structural mutant Hemoglobin Suan‐Dok (α2 109Leu→Arg). Blood 1990; 76(12)2630–2636