Diagnostic pitfall in PCR-based α-thalassemia genotyping resulting from a (G→C) polymorphism at nucleotide 71 3′ to the α2-globin gene termination codon [2]

بواسطة Chan, A.Y.-Y., Chan, L.-C., Luo, H.-Y., Chui, D.H.K., Wang, W., Chong, S.S., Ma, E.S.-K.
منشور في 2011

Determining the cause of patchwork HBA1 and HBA2 genes: Recurrent gene conversion or crossing over fixation events

بواسطة Law, H.-Y., Ng, I.S.L., Luo, H.-Y., Steinberg, M.H., Chui, D.H.K., Wang, W., Ho, J.F.V., Chong, S.S., Najmabadi, H.
منشور في 2011