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- W2012208175 abstract "β-Thalassemia (thal) patients with both α and β hemoglobin (Hb) variant genotypes are very rare. We recently studied a Taiwanese family in which the mother was a carrier of β-thal with an α chain v..." @default.
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- W2012208175 date "2002-01-01" @default.
- W2012208175 modified "2023-09-25" @default.
- W2012208175 title "Hb G-HONOLULU [α30(B11)Glu→Gln (α2)], Hb J-MEINUNG [β56(D7)Gly→Asp], ANDβ-THALASSEMIA [CODONS 41/42 (—TCTT)] IN A TAIWANESE FAMILY" @default.
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- W2012208175 doi "https://doi.org/10.1081/hem-120015039" @default.
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