Fig. 7From: Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China(a) MLPA analysis showing half dosages for two probes located in HBG1 in patient 2 and fourteen probes located in the HBB and HBD region in patient 2; (b) MLPA analysis showing half dosages for two probes located in HBG1 in patient 3Back to article page