Immunohematology (46)
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RH gene inversion-recombination as a major mechanism of the D-- phenotype in China
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Molecularly confirmed para-Bombay (Ah) secretor phenotype with FUT1 c.328G>A and FUT2 c.357C>T mutations: first case report from India
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Complete D epitope expression of the most common weak D types 15, 25, 33, and 72 in the Chinese population
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Neonatal alloimmune thrombocytopenia due to anti-HPA-1b and anti-HLA antibodies: diagnostic and transfusion management of a clinical case
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Multicenter evaluation of soluble CD38: neutralizing anti-CD38 pan-reactivity to enable alloantibody detection
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Passive transfer of silent red blood cell autoantibodies via the placenta and breast milk: a case report
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Non-invasive fetal HPA genotyping by UMI-NGS: a robust method for antenatal diagnosis including 48 fetal DNA markers
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A novel A allele with c.575T>C variant in glycosyltransferase A leads to ABO discrepancy
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Delayed hemolytic transfusion reaction associated with anti-Au(a) antibody in a young male with beta-thalassemia
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Molecular characterization of variant D antigen expression among 56,445 blood donors in East India
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When is ABO-incompatible plasma safe to transfuse? Defining an empirical estimation of anti-A/anti-B in ABO incompatible plasma-containing blood products
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Partial s antigen expression in GP(B-A-B) hybrid glycophorins and the corresponding in vitro expression study
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Post-transplant pediatric autoimmune hemolytic anemia: donor vs donor or recipient vs self?
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Identification of a novel ABO*O.01.01 allele with c.801G>T mutation in a Chinese A2 subtype individual
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Rh disease in Mexico: evaluating regional and institutional differences in treatment availability and disease management
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CD36 antibodies in isoimmunised African-origin pregnant women: three years experience in Spain
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ELP protocol: an original approach for the mitigation of anti-CD38 interference
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A case of trisomy 9 with mixed-field ABO blood type
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Description of the first case of c.137-8C>T GYPB mutation not associated to the GYPB(P2) allele
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Defining the breakpoints of hybrid blood group alleles
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Single-exon fetal RHD genotyping: a 31-month follow up in the obstetric population of Western Sweden
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Patients with red cell antibodies: registries improve patient care by increasing patient safety, reducing costs, and enabling health information exchange
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Genomic characterisation of clinically significant blood group variants in Aboriginal Australians
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Identification of the novel c.300C>G variation on the ABO*A1.02 allele associated with an AweakB phenotype
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Noninvasive fetal blood group antigen genotyping
46 Items