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.
The production, serologic evaluation, and epitope mapping of ten murine monoclonal Dombrock antibodies
Grodecka, M., Wasniowska, K., Halverson, G., Yazdanbakhsh, K., Reid, M.E., Lisowska, E.
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.
Cromer-related blood group antigens and the glycosyl phosphatidylinositol-linked protein, decay-accelerating factor DAF (CD55)
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.
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.
Practical method for determination of the U status of S–s– erythrocytes
Reid, M.E., Storry, J.R., Maurer, J., Nance, S.T.
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.