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Article | 17-February-2021

Clinical impacts of DNA-based typing and provision of antigen-matched red blood cell units for chronically transfused patients with thalassemia

is inaccurate because of the contaminating donor erythrocytes in patient circulation. DNA-based typing is superior in situations of recent transfusions.8 Moreover, it can guide the antigen-matched transfusion in individual patients. Furthermore, autoantibodies are frequently found in patients with thalassemia, causing crossmatch problems.9 The prevalence of autoantibodies is 0.47–28.2 percent by direct antiglobulin test and 57.6 percent by flow cytometry depending on study population and

P. Watanaboonyongcharoen, S. Onspun, P. Rojnuckarin

Immunohematology, Volume 36 , ISSUE 4, 137–145

Article | 26-October-2019

An overview of the Progenika ID CORE XT: an automated genotyping platform based on a fluidic microarray system

Mindy Goldman, Núria Nogués, Lilian M. Castilho

Immunohematology, Volume 31 , ISSUE 2, 62–68

Report | 20-March-2020

A simple screening assay for the most common JK*0 alleles revealed compound heterozygosity in Jk(a–b–) probands from Guam

not routinely available. Identification of Jk(a–b–) patients and donors is most often performed serologically. However, ten JK*0 alleles have been identified, and this information can be used in DNA-based typing. We selected five JK*0 alleles that had been encountered by our reference laboratory in two or more samples from unrelated individuals and designed an allele-specific primer PCR assay for use as an initial screening tool. After in-house validation, we tested genomic DNA from a

Elisabet Sjöberg Wester, Julia Gustafsson, Beverly Snell, Peggy Spruell, Åsa Hellberg, Martin L. Olsson, Jill R. Storry

Immunohematology, Volume 25 , ISSUE 4, 165–169

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