RH genotyping by nonspecific quantitative next‐generation sequencing von Stef, Marianne, Fennell, Katie, Apraiz, Izaskun, Arteta, David, González, Cecilia, Nogués, Nuria, Ochoa‐Garay, Gorka

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Three novel Er blood group system alleles and insights from protein modeling von Lane, William J., Vege, Sunitha, Mah, Helen H., Ochoa‐Garay, Gorka, Lomas‐Francis, Christine, Westhoff, Connie M.

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Uncommon S–s–U+ phenotype encoded by two novel GYPB alleles von Lomas‐Francis, Christine, Vege, Sunitha, Fuertes, June, Burgos, Anna, Tahiri, Toufik, Blackman, Moriah, Gannett, Michael, Ochoa‐Garay, Gorka, Westhoff, Connie M.

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Two novel variants that disrupt the RHCE start codon with varying effect on RhCE antigen expression von Vege, Sunitha, Floch, Aline, Burgos, Anna, Tahiri, Toufik, Kirkegaard, Julie, Dupont, Megan, Ochoa‐Garay, Gorka, Lomas‐Francis, Christine, Westhoff, Connie M.

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Four novel ABOAW alleles associated with weak antigen expression von Tahiri, Toufik, Vege, Sunitha, Floch, Aline, Lomas‐Francis, Christine, Ochoa‐Garay, Gorka, Westhoff, Connie M.

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An intron c.149‐2632T>A change in RHD is associated with aberrant transcription and very weak D phenotype von Floch, Aline, Vege, Sunitha, Berardi, Philip, Hannon, Judith, Ochoa‐Garay, Gorka, Lomas‐Francis, Christine, Westhoff, Connie M.

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Novel KEL02N allele in Saudi Arabia encoding a Kell null (K0) phenotype von Albasri, Jasem, Alsuhaibani, Omar, Almarry, Noorah, Ochoa‐Garay, Gorka, Bensing, Kathleen M., Biese, Danielle, Knier, Madeline, Denomme, Gregory A.

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A GYPB variant encoding an altered leader peptide leads to a weak S phenotype von Cote, Jacqueline, Cen, Selena, Fennell, Katie, Pambrun, Chantale, Branch, Donald R., Ochoa‐Garay, Gorka

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Two new RHD alleles with deletions spanning multiple exons von Matteocci, Antonella, Monge‐Ruiz, Jorge, Stef, Marianne, Apraiz, Izaskun, Herrera‐del‐Val, Lara, Mancuso, Tommaso, Fennell, Katie, Lopez, Monica, Larizgoitia‐Martin, Yolanda, Nespoli, Guido, Rubia‐Tejero, Montserrat, Collaretti, Angela, Pierelli, Luca, Ochoa‐Garay, Gorka

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Effect on gene expression of three allelic variants in GATA motifs of ABO, RHD, and RHCE regulatory elements von Fennell, Katie, Hoffman, Roser, Yoshida, Ken, Iwamoto, Sadahiko, Govender, Lavendri, Vather, Kuben, Sookraj, Ashika, Jentsch, Ute, Pambrun, Chantale, McAuley, Catherine, Keller, Margaret A., Ochoa‐Garay, Gorka

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Three new alleles encoding an apparent Kellnull phenotype von Puente, Fernando, Cemborain‐Garcia, Arantxa, Rodriguez‐Wilhelmi, Pablo, Garcia‐Sanchez, Felix, Rodriguez, Miguel‐Angel, Lucea, Irene, Ochoa‐Garay, Gorka

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FYA silencing by the GATA-motif variant FYA(−69C) in a Caucasian family von Písačka, Martin, Marinov, Iuri, Králová, Miroslava, Králová, Jana, Kořánová, Michaela, Bohoněk, Miloš, Sood, Chhavi, Ochoa-Garay, Gorka

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Identification of new KLF1 and LU alleles during the resolution of Lutheran typing discrepancies von Garcia-Sanchez, Felix, Pardi, Cecilia, Kupatawintu, Pawinee, Thornton, Nicole, Rodriguez, Miguel-Angel, Lucea, Irene, Sood, Chhavi, Ochoa-Garay, Gorka

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New RHD variant alleles von Garcia, Felix, Rodriguez, Miguel-Angel, Goldman, Mindy, Azcarate, Maria-Nerea, Rodriguez, Maria-Inmaculada, Muniz-Diaz, Eduardo, Puente, Fernando, Alshatti, Hana, Haimila, Katri, Molano, Araitz, Garaizar, Adirane, Ochoa-Garay, Gorka

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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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Three new alleles encoding an apparent Kell null phenotype von Puente, Fernando, Cemborain-Garcia, Arantxa, Rodriguez-Wilhelmi, Pablo, Garcia-Sanchez, Felix, Rodriguez, Miguel-Angel, Lucea, Irene, Ochoa-Garay, Gorka

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New RHCE variant alleles encoding the D- - phenotype von Ochoa-Garay, Gorka, Moulds, Joann M., Cote, Jacqueline, Kresie, Lesley, Garaizar, Adirane, Goldman, Mindy, Wynn, Polly

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Identification of six new RHCE variant alleles in individuals of diverse racial origin von Goldman, Mindy, Cemborain, Arantxa, Cote, Jacqueline, El Hamss, Rachid, Flower, Robert L., Garaizar, Adirane, Garcia-Sanchez, Felix, Hyland, Catherine A., Kalvelage, Monica, Londero, Donatella, Lopez, Genghis H., Revelli, Nicoletta, Rodriguez-Wilhelmi, Pablo, Villa, Antonietta, Ochoa-Garay, Gorka

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Strategy for managing maternal variant RHD alleles in Rhesus D negative obstetric populations during fetal RHD genotyping von Hyland, Catherine A., Gardener, Glenn J., O'Brien, Helen, Millard, Glenda, Gibbons, Kristen, Tremellen, Anne, Ochoa-Garay, Gorka, Flower, Robert L., Hyett, Jonathan A.

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Rh-null phenotype caused by a complete RHAG deletion von Gómez-Torreiro, Eduardo, Eiras-Martínez, Adolfo, Rodríguez-Calvo, María Inmaculada, Muñiz-Díaz, Eduardo, Nogués, Nuria, López, Mónica, Garaizar, Adirane, Ochoa-Garay, Gorka

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