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.
Anti-Uz found in mother’s serum and child’s eluate
Read, S.M., Taylor, M.M., Reid, M.E., Popovsky, M.A.
Review of a terminology proposed to supersede Miltenberger
Reid, M.E., Tippett, P.
Practical method for determination of the U status of S–s– erythrocytes
Reid, M.E., Storry, J.R., Maurer, J., Nance, S.T.
The second example of Lu:-7 phenotype: serology and immunochemical studies
Reid, M.E., Hoffer, J., Øyen, R., Tossas, E., Sadjadi, M., Messina, G.
En(a–)FIN phenotype in a Pakistani
Rapini, J., Batts, R., Yacob, M., Howard, C., Behzad, O., Singa, P., Walker, P.S., Reid, M.E.
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.
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.
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.