Multiple minisequencing screen for seven Southeast Asian nondeletional α-thalassemia mutations

بواسطة Wang, W., Chong, S.S., Ma, E.S.K., Chan, A.Y.Y., Chui, D.H.K.
منشور في 2013

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

Single-tube multiplex-PCR screen for anti-3.7 and anti-4.2 α-globin gene triplications

بواسطة Wang, W., Chong, S.S., Ma, E.S.K., Chan, A.Y.Y., Chan, L.C., Chui, D.H.K., Prior, J., Erber, W.N.
منشور في 2013

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

MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis

بواسطة Ding C., Chiu R.W.K., Lau T.K., Leung T.N., Chan L.C., Chan A.Y.Y., Charoenkwan P., Ng I.S.L., Law H.-Y., Ma E.S.K., Xu X., Wanapirak C., Sanguansermsri T., Liao C., Tan Jin Ai M.A., Chui D.H.K., Cantor C.R., Lo Y.M.D.
منشور في 2014