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

A Natiq, PA Lysy, Nynke Gillemans, R Schaap, A Sefiani, S Amzazi, SC El-Alaoui, Ileana Cantu, Bella Banjanin, Kirsten van Lom, CL Harteveld, Sjaak Philipsen

Research output: Contribution to journalArticleAcademicpeer-review

5 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)E2-E3
JournalAmerican Journal of Hematology
Issue number1
Publication statusPublished - 2017

Research programs

  • EMC OR-01

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