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Immunohematology|September 18, 2004
Studies on the Dombrock blood group system in non-human primatesC Mogos, A Schawalder, G R Halverson, et al.
Immunohematology|January 1, 1996
Effect of pronase on high-incidence blood group antigens and the prevalence of antibodies to pronase-treated erythrocytesM E Reid, C A Greeen, J Hoffer, et al.
American Journal of Human Genetics|December 1, 1987
Inheritance of human-erythrocyte Gerbich blood group antigensM E Reid, C Sullivan, M Taylor, et al.
Transfusion|December 22, 1999
Evidence for a separate genetic origin of the partial D phenotype DBT in a Japanese familyC H Huang, Y Chen, M E Reid, et al.
Immunohematology|June 1, 1992
A Polynesian family showing co-dominant inheritance of normal glycophorin C and the Gerbich variant form of glycophorin CM E Reid, J Poole, Y W Liew, et al.
Transfusion|May 29, 2000
Identification of a novel hybrid glycophorin gene encoding GP.HopJ R Storry, J Poole, J Condon, et al.
Transfusion|November 1, 1994
Duplication of exon 3 in the glycophorin C gene gives rise to the Lsa blood group antigenM E Reid, W Mawby, M J King, et al.
Immunohematology|September 18, 2004
Loss of enzyme-sensitive antigens due to the presence of leukocytes, neomycin sulfate, and LISSR W Velliquette, P Howard, H Malyska, et al.
Blood|July 10, 1998
Rhnull disease: the amorph type results from a novel double mutation in RhCe gene on D-negative backgroundC H Huang, Y Chen, M E Reid, et al.
American Journal of Human Genetics|January 23, 1999
Rhmod syndrome: a family study of the translation-initiator mutation in the Rh50 glycoprotein geneC Huang, G J Cheng, M E Reid, et al.
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