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- W1997747621 abstract "The term δβ-thalassemia with normal HbF has been recently proposed to define heterogenous δ and β globin gene molecular defects involving the same chromosome in cis. Here, we describe a Sardinian family in which three members showing microcytosis, border-line HbA2 levels and normal HbF proved to be heterozygotes for δ +27 and β°39 point mutations in cis by allele specific oligonucleotyde hybridization as well as by ECO 0 109 I endonuclease digestion and electrophoresis. As some of these β-thalassemia carriers shows normal HbA2 levels, knowledge of the molecular basis of this novel δβ-thalassemia silent phenotype would be useful in thalassemia screening and genetic counselling. © 1994 Wiley-Liss, Inc." @default.
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- W1997747621 date "1994-01-01" @default.
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- W1997747621 title "A novel mediterranean “δβ-thalassemia” determinant containing the δ+27 and β°39 point mutations in cis" @default.
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- W1997747621 doi "https://doi.org/10.1002/ajh.2830450113" @default.
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