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

Natiq, Abdelhafid; Lysy, Philippe; Gillemans, Nynke; Schaap, Rianne; Sefiani, Abdelaziz; Amzazi, Saaid; Chafai El-Alaoui, Siham; Cantú, Ileana; Banjanin, Bella; van Lom, Kirsten; Harteveld, Cornelis L; Philipsen, Sjaak

doi:10.1002/ajh.24574

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

Natiq, Abdelhafid

;

Lysy, Philippe

;

Gillemans, Nynke

;

Schaap, Rianne

;

Philipsen, Sjaak

;et.al.

(2017) American Journal of Hematology — Vol. 92, n° 1, p. E2-E3 (2017)

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Authors

Natiq, Abdelhafid
Author
Lysy, PhilippeUCLouvain
Author
Gillemans, Nynke
Author
Schaap, Rianne
Author
Philipsen, Sjaak
Author

Affiliations

UCLouvain(SLuc) Service d'endocrinologie et diabétologie pédiatrique
UCLouvainSSS/IREC/PEDI - Pôle de Pédiatrie

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Natiq, A., Lysy, P., Gillemans, N., Schaap, R., Sefiani, A., Amzazi, S., Chafai El-Alaoui, S., Cantú, I., Banjanin, B., van Lom, K., Harteveld, C. L., & 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. https://doi.org/10.1002/ajh.24574 (Original work published 2017)