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.
Liss-dependent autoantibody with apparent anti-U specificity
Chiofolo, J.T., Reid, M.E., Charles-Pierre, D.
The second example of Lu:-7 phenotype: serology and immunochemical studies
Reid, M.E., Hoffer, J., Øyen, R., Tossas, E., Sadjadi, M., Messina, G.
Characterization of human anti-hrB-like monoclonal antibody
Blancher, A.P., Reid, M.E., Alié-Daram, S.J., Dugoujon, J-M.H., Roubinet, F.L.
Effect of pronase on high-incidence blood group antigens and the prevalence of antibodies to pronase-treated erythrocytes
Reid, M.E., Green, C.A., Hoffer, J., Øyen, R.
Practical method for determination of the U status of S–s– erythrocytes
Reid, M.E., Storry, J.R., Maurer, J., Nance, S.T.
Moderate hemolytic disease of the newborn (HDN) due to anti-Rh17 produced by a black female with an e variant phenotype
Brumit, M.C., Carnahan, G.E., Stubbs, J.R., Storry, J.R., Reid, M.E.
MIMA-9, a valuable antibody for screening for rare donors
Tossas, E., Øyen, R., Halverson, G.R., Malyska, H., Reid, M.E.