Anti-N antibody mimicking an antibody to a high frequency antigen in a U-negative patient von Revoltar, Maxine, Clarke, Lisa, Bruce, Hayley, Liew, Yew Wah, Lopez, Genghis H

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Feasibility for non‐invasive prenatal fetal blood group and platelet genotyping by massively parallel sequencing: A single test system for multiple atypical red cell, platelet and... von McGowan, Eunike C., O'Brien, Helen, Sarri, Mia E., Lopez, Genghis H., Daly, James J., Flower, Robert L., Gardener, Glenn J., Hyland, Catherine A.

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Evaluation of targeted exome sequencing for 28 protein‐based blood group systems, including the homologous gene systems, for blood group genotyping von Schoeman, Elizna M., Lopez, Genghis H., McGowan, Eunike C., Millard, Glenda M., O'Brien, Helen, Roulis, Eileen V., Liew, Yew‐Wah, Martin, Jacqueline R., McGrath, Kelli A., Powley, Tanya, Flower, Robert L., Hyland, Catherine A.

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Recurrent pregnancy loss in a patient with anti-Rh17 von Moiz, Bushra, Salman, Muhammed, Rasheed, Seher, Qudus, Ruhul, Millard, Glenda, Hyland, Catherine A, Flower, Robert L, Wilson, Brett, Turner, Robyn, Lopez, Genghis H, Liew, Yew-Wah

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A cold case of hemolytic disease of the fetus and newborn resolved by genomic sequencing and population studies to define a new antigen in the Rh system von Wilson, Brett, Davison, Candice L., Lopez, Genghis H., Millard, Glenda M., Liew, Yew‐Wah, Powley, Tanya, Campbell, Tamika, Jadhao, Sudhir S., Nagaraj, Shivashankar H., Perry, Maree, Roulis, Eileen V., Toombs, Maree, Irving, David O., Flower, Robert L., Hyland, Catherine A.

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Fatal haemolytic transfusion reaction due to anti‐Ena and identification of a novel GYPA c.295delG variant in a Thai family von Suwanwootichai, Ploymanee, Lopez, Genghis H., Emthip, Morakot, Wilson, Brett, Millard, Glenda M., Onpuns, Sunisa, Laemsri, Kanchana, Bejrachandra, Sasitorn, Liew, Yew‐Wah

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Hemolytic disease of the fetus and newborn caused by anti‐sD antibody in a GP.Mur/Mur Thai mother and review of the prevalence of sD in Thai blood donors von Lopez, Genghis H., Emthip, Morakot, Suwanwootichai, Ploymanee, Millard, Glenda M., Wilson, Brett, Onpuns, Sunisa, Laemsri, Kanchana, Chiewsilp, Pimol, Flower, Robert L., Hyland, Catherine A., Liew, Yew‐Wah

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A Bioinformatically Initiated Approach to Evaluate GATA1 Regulatory Regions in Samples with Weak D, Del, or D– Phenotypes Despite Normal RHD Exons von McGowan, Eunike C., Wu, Ping Chun, Hellberg, Åsa, Lopez, Genghis H., Hyland, Catherine A., Olsson, Martin L.

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Genotyping analysis of MNS blood group GP(B‐A‐B) hybrid glycophorins in the Chinese Southern Han population using a high‐resolution melting assay von Wei, Ling, Lopez, Genghis H., Zhang, Yang, Wen, Jizhi, Wang, Zhen, Fu, Yongshui, Hyland, Catherine A., Flower, Robert L., Luo, Guangping, Ji, Yanli

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A new high‐prevalence LW antigen detected by an antibody in an Indigenous Australian homozygous for LWA c.309C>A variant von Lopez, Genghis H., Wilson, Brett, Millard, Glenda M., Cawthorne, Tanya L., Grey, Dianne E., Fong, Elizabeth A., Flower, Robert L., Hyland, Catherine A., Liew, Yew‐Wah

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Targeted exome sequencing defines novel and rare variants in complex blood group serology cases for a red blood cell reference laboratory setting von Schoeman, Elizna M., Roulis, Eileen V., Liew, Yew‐Wah, Martin, Jacqueline R., Powley, Tanya, Wilson, Brett, Millard, Glenda M., McGowan, Eunike C., Lopez, Genghis H., O'Brien, Helen, Condon, Jennifer A., Flower, Robert L., Hyland, Catherine A.

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An alloantibody in a homozygous GYPMur individual defines JENU (MNS49), a new high‐frequency antigen on glycophorin B von Lopez, Genghis H., Wilson, Brett, Liew, Yew‐Wah, Kupatawintu, Pawinee, Emthip, Morakot, Hyland, Catherine A., Flower, Robert L.

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Anti‐D in a mother, hemizygous for the variant RHDDNB gene, associated with hemolytic disease of the fetus and newborn von Quantock, Kelli M., Lopez, Genghis H., Hyland, Catherine A., Liew, Yew‐Wah, Flower, Robert L., Niemann, Frans J., Joyce, Arthur

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Non-invasive fetal RHD genotyping for RhD negative women stratified into RHD gene deletion or variant groups: comparative accuracy using two blood collection tube types von Hyland, Catherine A., Millard, Glenda M., O'Brien, Helen, Schoeman, Elizna M., Lopez, Genghis H., McGowan, Eunike C., Tremellen, Anne, Puddephatt, Rachel, Gaerty, Kirsten, Flower, Robert L., Hyett, Jonathan A., Gardener, Glenn J.

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Frequency of Mia (MNS7) and Classification of Mia-Positive Hybrid Glycophorins in an Australian Blood Donor Population von Lopez, Genghis H., Wilson, Brett, Turner, Robyn M., Millard, Glenda M., Fraser, Nicole S., Roots, Naomi M., Liew, Yew-Wah, Hyland, Catherine A., Flower, Robert L.

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Modified expression of the KEL2 (k) blood group antigen attributed to p.Leu196Val amino acid change three residues from the K/k antigen polymorphism site: implications for donor sc... von Millard, Glenda M., Lopez, Genghis H., Turner, Elise M., Lizarazu, Maria E., Roots, Naomi M., Liew, Yew‐Wah, Flower, Robert L., Hyland, Catherine A.

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A DEL phenotype attributed to RHD Exon 9 sequence deletion: slipped‐strand mispairing and blood group polymorphisms von Lopez, Genghis H., Turner, Robyn M., McGowan, Eunike C., Schoeman, Elizna M., Scott, Stacy A., O'Brien, Helen, Millard, Glenda M., Roulis, Eileen V., Allen, Amanda J., Liew, Yew‐Wah, Flower, Robert L., Hyland, Catherine A.

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GYPKip, a novel GYP(B-A-B) hybrid allele, encoding the MNS48 (KIPP) antigen von Lopez, Genghis H., Wei, Ling, Ji, Yanli, Condon, Jennifer A., Luo, Guangping, Hyland, Catherine A., Flower, Robert L.

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Frequency of Mi(a)(MNS7) and Classification of Mi(a)-Positive Hybrid Glycophorins in an Australian Blood Donor Population von Lopez, Genghis H., Wilson, Brett, Turner, Robyn M., Millard, Glenda M., Fraser, Nicole S., Roots, Naomi M., Liew, Yew-Wah, Hyland, Catherine A., Flower, Robert L.

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Genotyping by sequencing defines independent novel RHD variants for an antenatal patient and a blood donor von Lopez, Genghis H., McGowan, Eunike C., Condon, Jennifer A., Schoeman, Elizna M., Millard, Glenda M., O'Brien, Helen, Roulis, Eileen V., Ochoa‐Garay, Gorka, Liew, Yew‐Wah, Flower, Robert L., Hyland, Catherine A.

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