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Hereditary persistence of fetal hemoglobin in two patients with KLF1 haploinsufficiency due to 19p13.2–p13.12/13 deletion

American Journal of Hematology
DOI: 10.1002/ajh.24574
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Natiq, A., Lysy, P. A., Gillemans, N., Schaap, R., Sefiani, A., Amzazi, S., … Philipsen, S. (2017, January 1). Hereditary persistence of fetal hemoglobin in two patients with KLF1 haploinsufficiency due to 19p13.2–p13.12/13 deletion. American Journal of Hematology. Wiley-Liss Inc. https://doi.org/10.1002/ajh.24574

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