Prevalence of RHD*DOL and RHCE*ce(818T) in two populations
Halter Hipsky, C., da Costa, D.C., Omoto, R., Zanette, A., Castilho, L., Reid, M.E.
Molecular background of RH in Bastiaan, the RH:–31,–34 index case, and two novel RHD alleles
Reid, M.E., Hipsky, C.H., Velliquette, R.W., Lomas-Francis, C., Larimore, K., Olsen, C.
A review of the JR blood group system
Castilho, L., Reid, M.E.
SC*994C>T causes the Scnull phenotype in Pacific Islanders and successful transfusion of Sc3+ blood to a patient with anti-Sc3
Hue-Roye, K., Velliquette, R.W., Larimore, K., Moscarelli, S., Ohswaldt, N., Lomas-Francis, C., Reid, M.E.
A Polynesian family showing co-dominant inheritance of normal glycophorin C and the Gerbich variant form of glycophorin C
Reid, M.E., Poole, J., Liew, Y.W., Pinder, L.
Review: the Diego blood group system
Zafar, M., Reid, M.E.
Possible suppression of fetal erythropoiesis by the Kell blood group antibody anti-Kpa
Tuson, M., Hue-Roye, K., Koval, K., Imlay, S., Desai, R., Garg, G., Kazem, E., Stockman, D., Hamilton, J., Reid, M.E.