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.
The gene encoding the I blood group antigen: review of an I for an eye
Reid, M.E.
Cefotetan-induced immune hemolytic anemia following prophylaxis for cesarean delivery
Shariatmadar, S., Storry, J.R., Sausais, L., 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.
Loss of enzyme-sensitive antigens due to the presence of leukocytes, neomycin sulfate, and LISS
Velliquette, R.W., Howard, P., Malyska, H., Reid, M.E.
Molecular studies of DO alleles reveal that JO is more prevalent than HY in Brazil, whereas HY is more prevalent in New York
Castilho, L., Baleotti, W., Tossas, E., Hue-Roye, K., Ribeiro, K.R., Lomas-Francis, C., Charles-Pierre, D., Reid, M.E.
RHD deletion in a patient with chronic myeloid leukemia
Murdock, A., Assip, D., Hue-Roye, K., Lomas-Francis, C., Hu, Z., Vege, S., Westhoff, C.M., 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.
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.
The polymorphism nt 76 in exon 2 of SC is more frequent in Whites than in Blacks
Fuchisawa, A., Lomas-Francis, C., Hue-Roye, K., Reid, M.E.
Consortium for Blood Group Genes (CBGG): 2009 report
Denomme, G.A., Westhoff, C.M, Castilho, L.M., St-Louis, M., Castro, V., Reid, M.E.
RHCE*ceAR encodes a partial c (RH4) antigen
Halter Hipsky, C., Lomas-Francis, C., Fuchisawa, A., Reid, M.E.