Diverse and novel RHD variants in Australian blood donors with a weak D phenotype: implication for transfusion management von McGowan, E. C., Lopez, G. H., Knauth, C. M., Liew, Y.‐W., Condon, J. A., Ramadi, L., Parsons, K., Turner, E. M., Flower, R. L., Hyland, C. A.

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Duffy blood group phenotype-genotype correlations using high-resolution melting analysis PCR and microarray reveal complex cases including a new null FYA allele: the role for seque... von Lopez, G. H., Morrison, J., Condon, J. A., Wilson, B., Martin, J. R., Liew, Y.-W., Flower, R. L., Hyland, C. A.

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Vox Sanguinis International Forum on application of fetal blood grouping von Daniels, G., Finning, K., Lozano, M., Hyland, C. A., Liew, Y.‐W., Powley, T., Castilho, L., Bonet Bub, C., Kutner, J. M., Banch Clausen, F., Christiansen, M., Sulin, K., Haimila, K., Legler, T. J., Lambert, M., Ryan, H., Ní Loingsigh, S., Matteocci, A., Pierelli, L., Dovc Drnovsek, T., Bricl, I., Nogués, N., Muñiz‐Diaz, E., Olsson, M. L., Wikman, A., Haas, M., Schoot, C. E., Massey, E., Westhoff, C. M.

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Vox Sanguinis International Forum on application of fetal blood grouping: summary von Daniels, G., Finning, K., Lozano, M., Hyland, C. A., Liew, Y.‐W., Powley, T., Castilho, L., Bonet Bub, C., Kutner, J. M., Banch Clausen, F., Christiansen, M., Sulin, K., Haimila, K., Legler, T. J., Lambert, M., Ryan, H., Ní Loingsigh, S., Matteocci, A., Pierelli, L., Dovc Drnovsek, T., Bricl, I., Nogués, N., Muñiz‐Diaz, E., Olsson, M. L., Wikman, A., Haas, M., Schoot, C. E., Massey, E., Westhoff, C. M.

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A novel FYA allele with the 265T and 298A SNPs formerly associated exclusively with the FYB allele and weak Fy(b) antigen expression: implication for genotyping interpretative algo... von Lopez, G H, Condon, J A, Wilson, B, Martin, J R, Liew, Y-W, Flower, R L, Hyland, C A

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Prenatal RHD gene determination and dosage analysis by PCR: clinical evaluation von Chan, F.-Y., Cowley, N. M., Wolter, L., Stone, M., Carmody, F., Saul, A., Hyland, C. A.

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Three unrelated Rh D gene polymorphisms identified among blood donors with rhesus CCee (r'r') phenotypes von HYLAND, C. A, WOLTER, L. C, SAUL, A

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A novel FYA allele with the 265T and 298A SNPs formerly associated exclusively with the FYB allele and weak Fyb antigen expression: implication for genotyping interpretative algori... von Lopez, G. H., Condon, J. A., Wilson, B., Martin, J. R., Liew, Y.-W., Flower, R. L., Hyland, C. A.

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Exposure to GB virus type C or hepatitis G virus in selected Australian adult and children populations von Hyland, C. A., Mison, L., Solomon, N., Cockerill, J., Wang, L., Hunt, J., Selvey, L. A., Faoagali, J., Cooksley, W. G. E., Young, I. F., Trowbridge, R., Borthwick, I., Gowans, E. J.

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Blood group genotype analysis of Australian reagent red blood cell donors across three genotyping platforms: consistent detection of 7·0% phenotype genotype nonconcordance von McBean, R. S., Hyland, C. A., Davis, A. C., Condon, J., Parsons, K., Flower, R. L.

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Prevalence of hepatitis C virus and genotype distribution in an Australian volunteer blood donor population von Mison, L.M., Young, I.F., O'Donoghue, M., Cowley, N., Thorlton, N., Hyland, C.A.

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Is there evidence for vector transmission of GBV-C? von Selvey, LA, Hyland, CA, Mison, L, Solomon, N, Gowans, EJ

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RHESUS D GENOTYPING USING POLYMERASE CHAIN REACTION von Wolter, Lindsay C., Hyland, Catherine A., Saul, Allan

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A southern analysis of Rh blood group genes : association between restriction fragment length polymorphism patterns and Rh serotypes von HYLAND, C. A, WOLTER, L. C, LIEW, Y.-W, SAUL, A

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Biobanks of blood from donors and recipients of blood products von Reesink, H. W., Engelfriet, C. P., Hyland, C. A., Coghlan, P., Tait, B., Wsolak, M., Keller, A. J., Henn, G., Mayr, W. R., Thomas, I., Osselaer, J.-C., Lambermont, M., Beaten, M., Wendel, S., Qiu, Y., Georgsen, J., Krusius, T., Mäki, T., Andreu, G., Morel, P., Lefrère, J.-J., Rebulla, P., Giovanelli, S., Butti, B., Lecchi, L., Mozzi, F., Van Hilten, J. A., Zwaginga, J. J., Flanagan, P., Flesland, Ø., Brojer, E., Łętowska, M., Åkerblom, O., Norda, R., Prowse, C., Dow, B., Jarvis, L., Davidson, F., Kleinman, S., Bianco, C., Stramer, S. L., Dodd, R. Y., Busch, M. P.

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The RhD- trait in a white patient with the RhCCee phenotype attributed to a four-nucleotide deletion in the RHD gene von Andrews, K T, Wolter, L C, Saul, A, Hyland, C A

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Identification and analysis of Rh genes: Application of PCR and RFLP typing tests von Hyland, Catherine A., Wolter, Lindsay C., Saul, Allan

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A novel FY A allele with the 265T and 298A SNP s formerly associated exclusively with the FY B allele and weak Fy b antigen expression: implication for genotyping interpretative al... von Lopez, G. H., Condon, J. A., Wilson, B., Martin, J. R., Liew, Y.‐W., Flower, R. L., Hyland, C. A.

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Duffy blood group phenotype–genotype correlations using high‐resolution melting analysis PCR and microarray reveal complex cases including a new null FY A allele: the role for sequ... von Lopez, G. H., Morrison, J., Condon, J. A., Wilson, B., Martin, J. R., Liew, Y.‐W., Flower, R. L., Hyland, C. A.

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A novel single missense mutation identified along the RH50 gene in a composite heterozygous Rhnull blood donor of the regulator type von HYLAND, C. A, CHERIF-ZAHAR, B, COWLEY, N, RAYNAL, V, PARKES, J, SAUL, A, CARTRON, J. P

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