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Showing 37-48 of 55 for the term ""Reid, M.E.""

The second example of Lu:-7 phenotype: serology and immunochemical studies
Article

The second example of Lu:-7 phenotype: serology and immunochemical studies

Reid, M.E., Hoffer, J., Øyen, R., Tossas, E., Sadjadi, M., Messina, G.
En(a–)FIN phenotype in a Pakistani
Article

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.
Liss-dependent autoantibody with apparent anti-U specificity
Article

Liss-dependent autoantibody with apparent anti-U specificity

Chiofolo, J.T., Reid, M.E., Charles-Pierre, D.
Use of LOR-15C9 monoclonal anti-D to differentiate erythrocytes with the partial DVI antigen from those with other partial D antigens or weak D antigens
Article

Use of LOR-15C9 monoclonal anti-D to differentiate erythrocytes with the partial DVI antigen from those with other partial D antigens or weak D antigens

Reid, M.E., Halverson, G.R., Roubinet, F., Apoil, P.A., Blancher, A.
Characterization of human anti-hrB-like monoclonal antibody
Article

Characterization of human anti-hrB-like monoclonal antibody

Blancher, A.P., Reid, M.E., Alié-Daram, S.J., Dugoujon, J-M.H., Roubinet, F.L.
A second example of anti-Esa, an antibody to a high-incidence Cromer antigen
Article

A second example of anti-Esa, an antibody to a high-incidence Cromer antigen

Reid, M.E., Marfoe, R.A., Mueller, A.L., Arndt, P.A., Sausais, L., Spruell, P.
Glycophorin A-deficient red cells may have a weak expression of C4-bound Ch and Rg antigens
Article

Glycophorin A-deficient red cells may have a weak expression of C4-bound Ch and Rg antigens

Tippett, P., Storry, J.R., Walker, P.S., Okubo, Y., Reid, M.E.
Confirmation that the JAHK antigen is associated with the rG haplotype
Article

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
Article

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.
MIMA-9, a valuable antibody for screening for rare donors
Article

MIMA-9, a valuable antibody for screening for rare donors

Tossas, E., Øyen, R., Halverson, G.R., Malyska, H., Reid, M.E.
The Cromer blood group system: a review
Article

The Cromer blood group system: a review

Storry, J.R., Reid, M.E.
Studies on the Dombrock blood group system in non-human primates
Article

Studies on the Dombrock blood group system in non-human primates

Mogos, C., Schawalder, A., Halverson, G.R., Reid, M.E.