Review of a terminology proposed to supersede Miltenberger
Reid, M.E., Tippett, P.
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.
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.
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.
RHCE*ceAR encodes a partial c (RH4) antigen
Halter Hipsky, C., Lomas-Francis, C., Fuchisawa, A., 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.
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.
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.
Consortium for Blood Group Genes (CBGG): 2008 report
A. Denomme, G., Westhoff, C.M., 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.
Prevalence of RHD*DOL and RHCE*ce(818T) in two populations
Halter Hipsky, C., da Costa, D.C., Omoto, R., Zanette, A., Castilho, L., Reid, M.E.
The ISBT 700 series of low-incidence and 901 series of high-incidence blood group antigens
Reid, M.E.