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Showing 1-12 of 13 for the term ""Hue-Roye, K.""

Posttransplant maternal anti-D: a case study and review
Article

Posttransplant maternal anti-D: a case study and review

Senzel, L., Avila, C., Ahmed, T., Gill, H., Hue-Roye, K., Lomas-Francis, C., Reid, M.E.
The molecular basis of the LU:7 and LU:–7 phenotypes
Article

The molecular basis of the LU:7 and LU:–7 phenotypes

Hue-Roye, K., E. Reid, M.
Case report: DNA testing resolves unusual serologic results in the Dombrock system
Article

Case report: DNA testing resolves unusual serologic results in the Dombrock system

MacFarland, D., Hue-Roye, K., Carter, S., Moreau, D., Barry, J., Moulds, M.K., Lomas-Francis, C., Reid, M.E.
DNA analysis for donor screening of Dombrock blood group antigens
Article

DNA analysis for donor screening of Dombrock blood group antigens

Storry, J.R., Westhoff, C.M., Charles-Pierre, D., Rios, M., Hue-Roye, K., Vege, S., Nance, S., Reid, M.E.
An alloantibody to a high-prevalence MNS antigen in a person with a GP.JL/Mk phenotype
Article

An alloantibody to a high-prevalence MNS antigen in a person with a GP.JL/Mk phenotype

Ratliff, J., Veneman, S., Ward, J., Lomas-Francis, C., Hue-Roye, K., Velliquette, R.W, Sausais, L., Maldonado, T., Miyamoto, J., Martin, Y., Slater, D., Reid, M.E.
Analysis of SERF in Thai blood donors
Article

Analysis of SERF in Thai blood donors

Palacajornsuk, P., Hue-Roye, K., Nathalang, O., Tantimavanich, S., Bejrachandra, S., Reid, M.E.
Novel molecular basis of an Inab phenotype
Article

Novel molecular basis of an Inab phenotype

Hue-Roye, K., Powell, V.I., Patel, G., Lane, D., Maguire, M., Chung, A., 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
Article

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.
The polymorphism nt 76 in exon 2 of SC is more frequent in Whites than in Blacks
Article

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.
Principles of PCR-based assays
Article

Principles of PCR-based assays

Hue-Roye, K., Vege, S.
Possible suppression of fetal erythropoiesis by the Kell blood group antibody anti-Kpa
Article

Possible suppression of fetal erythropoiesis by the Kell blood group antibody anti-Kpa

Tuson, M., Hue-Roye, K., Koval, K., Imlay, S., Desai, R., Garg, G., Kazem, E., Stockman, D., Hamilton, J., Reid, M.E.
RHD deletion in a patient with chronic myeloid leukemia
Article

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.