A method to detect McLeod phenotype red blood cells
Øyen, R., Reid, M.E., Rubenstein, P., Ralph, H.
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.
Use of LOR-15C9 monoclonal anti-D to differentiate erythrocytes with the partial DVI antigen from those with other partial D antigens or weak D antigens
Reid, M.E., Halverson, G.R., Roubinet, F., Apoil, P.A., Blancher, A.
Practical method for determination of the U status of S–s– erythrocytes
Reid, M.E., Storry, J.R., Maurer, J., Nance, S.T.
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.
A second example of anti-Esa, an antibody to a high-incidence Cromer antigen
Reid, M.E., Marfoe, R.A., Mueller, A.L., Arndt, P.A., Sausais, L., Spruell, P.
The second example of Lu:-7 phenotype: serology and immunochemical studies
Reid, M.E., Hoffer, J., Øyen, R., Tossas, E., Sadjadi, M., Messina, G.
Glycophorin A-deficient red cells may have a weak expression of C4-bound Ch and Rg antigens
Tippett, P., Storry, J.R., Walker, P.S., Okubo, Y., Reid, M.E.
Liss-dependent autoantibody with apparent anti-U specificity
Chiofolo, J.T., Reid, M.E., Charles-Pierre, D.
ABO blood group system: a review of molecular aspects
Lee, A.H., Reid, M.E.
Confirmation that the JAHK antigen is associated with the rG haplotype
Kosanke, J., Storry, J.R., Reid, M.E.
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.