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.
A review of the JR blood group system
Castilho, L., Reid, M.E.
Value of DNA-based assays for donor screening and regulatory issues
Strauss, D., 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.
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.
MNS blood group system: a review
Reid, M.E.
A method to detect McLeod phenotype red blood cells
Øyen, R., Reid, M.E., Rubenstein, P., Ralph, H.
The Dombrock blood group system: a review
Lomas-Francis, C., 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.