HbS-Sicilian (δβ)0-Thalassemia: A Rare Variant of Sickle Cell
Article in Case Reports in Hematology (September 2017)
The most recent citing publications are shown below. View all 7 publications that cite this research output on Dimensions.
Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs
Article in Experimental Biology and Medicine (October 2016)
Screening for common β‐globin gene cluster deletions in Chinese individuals with increased hemoglobin F
Article in International Journal of Laboratory Hematology (July 2015)