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

2017

American Journal of Hematology , Volume 92 - Issue 1 p. E2- E3

Additional Metadata
Persistent URL	doi.org/10.1002/ajh.24574, hdl.handle.net/1765/94735
Journal	American Journal of Hematology
Organisation	Erasmus University Rotterdam
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Natiq, A. (Abdelhafid), Lysy, P. A., Gillemans, N., Schaap, R. (Rianne), Sefiani, A., Amzazi, S. (Saaid), … Philipsen, S. (2017). Hereditary persistence of fetal hemoglobin in two patients with KLF1 haploinsufficiency due to 19p13.2-p13.12/13 deletion. American Journal of Hematology, 92(1), E2–E3. doi:10.1002/ajh.24574

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