Prospective and retrospective primary prevention of hemoglobinopathies in multiethnic societies
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One-third of the new paediatric sickle cell disease patients in the Netherlands is an immigrant and does not benefit from neonatal screening
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Rapid detection of α-thalassaemia deletions and α-globin gene triplication by multiplex polymerase chain reactions
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Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies
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Known and new δ globin gene mutations and their diagnostic significance
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Occurrence of common and rare δ-globin gene defects in two multi ethnic populations: Thirteen new mutations and the significance of δ-globin gene defects in β-thalassemia diagnostics
(in press)
Phylipsen M, Gallivan MVE, Arkesteijn SGJ, Harteveld CL, Giordano PC. Occurrence of common and rare δ-globin gene defects in two multi ethnic populations: thirteen new mutations and the significance of δ-globin gene defects in β-thalassemia diagnostics. Int J Lab Hematol. 2010 (in press).