Výsledky vyhledávání - "Kelli A, McGrath"

Evaluation of targeted exome sequencing for 28 protein-based blood group systems, including the homologous gene systems, for blood group genotyping

Autor: Kelli A. McGrath, Elizna M. Schoeman, Catherine A. Hyland, Tanya Powley, Eileen Roulis, Helen O'Brien, Yew-Wah Liew, Genghis H. Lopez, Eunike C. McGowan, Jacqueline R. Martin, Robert L. Flower, Glenda M. Millard

Publikováno v: Transfusion. 57:1078-1088

BACKGROUND: Blood group single nucleotide polymorphism genotyping probes for a limited range of polymorphisms. This study investigated whether massively parallel sequencing (also known as next-generation sequencing), with a targeted exome strategy, p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7ee5c3efca0bfc310e7919b6d8652c6a
https://doi.org/10.1111/trf.14054

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A D+ blood donor with a novelRHD*D‐CE(5‐6)‐Dgene variant exhibits the low‐frequency antigen RH23 (DW) characteristic of the partial DVa phenotype

Autor: Elizna M. Schoeman, Maria E. Abaca‐Cleopas, Glenda M. Millard, Kelli A. McGrath, Yew-Wah Liew, Genghis H. Lopez, Helen O'Brien, Robert L. Flower, Eunike C. McGowan, Catherine A. Hyland

Publikováno v: Transfusion. 56:2322-2330

BACKGROUND: Blood donors whose red blood cells (RBCs) exhibit a partial RhD phenotype, lacking some D epitopes, present as D+ in routine screening. Such phenotypes can exhibit low-frequency antigens (LFAs) of clinical significance. The aim of this st

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efee21ce4eaf22a6737a5255ede92b68
https://doi.org/10.1111/trf.13713

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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

Autor: Elizna M, Schoeman, Genghis H, Lopez, Eunike C, McGowan, Glenda M, Millard, Helen, O'Brien, Eileen V, Roulis, Yew-Wah, Liew, Jacqueline R, Martin, Kelli A, McGrath, Tanya, Powley, Robert L, Flower, Catherine A, Hyland

Publikováno v: Transfusion. 57(4)

Blood group single nucleotide polymorphism genotyping probes for a limited range of polymorphisms. This study investigated whether massively parallel sequencing (also known as next-generation sequencing), with a targeted exome strategy, provides an e

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::379d0159aed34a146cf8ea4e2e233da7
https://pubmed.ncbi.nlm.nih.gov/28338218

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