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  1. G(HbF): A genetic model of fetal hemoglobin in sickle cell disease

    Fetal hemoglobin (HbF) is a strong modifier of sickle cell disease (SCD) severity and is associated with 3 common genetic loci. Quantifying the genetic effects of the 3 loci would specifically address the benefits of HbF increases in patients.

    http://iris.ucl.ac.uk/iris/publication/1711278/7

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