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- W2064758637 abstract "Hemoglobin Taybe is an unstable α-chain hemoglobin variant caused by a deletion of a threonine residue at codon 38 or 39 of the α-1 globin chain. We describe preterm infant triplets born with hydrops fetalis and anemia who were found by DNA analysis to be homozygous for hemoglobin Taybe. All three infants developed intrauterine hemolytic anemia, which subsequently led to hydrops fetalis. To the best of our knowledge, this is the first description of hydrops fetalis associated with this hemoglobinopathy. We suggest that hemoglobin Taybe be considered in the differential diagnosis of hydrops fetalis and that known affected fetuses be carefully followed both antenatally and postnatally. Am. J. Hematol. 76:263–266, 2004. © 2004 Wiley-Liss, Inc." @default.
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- W2064758637 date "2004-01-01" @default.
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- W2064758637 title "Hydrops fetalis associated with homozygosity for hemoglobin Taybe (? 38/39 THR deletion) in newborn triplets" @default.
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- W2064758637 doi "https://doi.org/10.1002/ajh.20094" @default.
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