Immunohematology (51)
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Identification of a novel B allele with c.298T>A giving rise to a weak B phenotype in Chinese voluntary blood donors
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Results of red cell antibody screening assays from 2,500 laboratories in 10 external quality assessment programs: sensitivity for anti-D
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Irregular antibodies in pregnancy during the universal anti-RHD prophylaxis era: a survey of Spanish Hospitals
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Identification and analysis of a novel ABO allele with c.959insC variant in a Chinese blood donor
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Molecular mechanism of a novel Aweak subtype in Chinese pedigrees: identification and analysis of a large genomic deletion in the promoter upstream distal region of the ABO gene
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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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Identification of a novel ABO*O.01.01 allele with c.801G>T mutation in a Chinese A2 subtype individual
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Post-transplant pediatric autoimmune hemolytic anemia: donor vs donor or recipient vs self?
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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
51 Items