Associated Papers
A novel RHCE*02 variant with a recombination of RHD exon 3 in a Chinese D+ voluntary blood donor with weak expression of e antigen.
Yang HM et al.
Transfusion, 2026
Rapid change in red cell blood group systems after the main Out of Africa of Homo sapiens.
Mazières S et al.
Scientific Reports, 2025
39848961 (PubMed )
Supplement: 41598_2024_83023_MOESM2_ESM.docx
Blood donor genotyping for prediction of blood group antigens: Results from 5 years' experience (2017-2022).
Rieneck K et al.
Vox Sanguinis, 2023
Optimization of diagnostic strategy for non-invasive cell-free foetal RHD determination from maternal plasma.
Pazourkova E et al.
Vox Sanguinis, 2021
A Review of the Literature Organized Into a New Database: RHeference.
Floch A et al.
Transfusion Medicine Reviews, 2021
The Significance of RHD Genotyping and Characteristic Analysis in Chinese RhD Variant Individuals.
Ying Y et al.
Frontiers in Immunology, 2021
Molecular basis and zygosity determination of D variants including identification of four novel alleles in Chinese individuals.
He J et al.
Transfusion, 2015
D category IV: a group of clinically relevant and phylogenetically diverse partial D.
von Zabern I et al.
Transfusion, 2013
RHD and RHCE variant and zygosity genotyping via multiplex ligation-dependent probe amplification.
Haer-Wigman L et al.
Transfusion, 2013
Partial D phenotypes and genotypes in the Chinese population.
Ye L et al.
Transfusion, 2012
Six years' experience performing RHD genotyping to confirm D- red blood cell units in Germany for preventing anti-D immunizations.
Flegel WA et al.
Transfusion, 2009
DCS-1, DCS-2, and DFV share amino acid substitutions at the extracellular RhD protein vestibule.
Flegel WA et al.
Transfusion, 2008
In-frame triplet deletions in RHD alter the D antigen phenotype.
Flegel WA et al.
Transfusion, 2006
Random survey for RHD alleles among D+ European persons.
Chen Q et al.
Transfusion, 2005
A D(V)-like phenotype is obliterated by A226P in the partial D DBS.
Wagner FF et al.
Transfusion, 2001
Molecular analysis of Rh transcripts and polypeptides from individuals expressing the DVI variant phenotype: an RHD gene deletion event does not generate All DVIccEe phenotypes.
Avent ND et al.
Blood, 1997
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