Associated Papers
Partial D variant with demonstrated risk of D alloimmunization in the Australian Indigenous population.
Palfreyman E et al.
Vox Sanguinis, 2025
Rapid change in red cell blood group systems after the main Out of Africa of Homo sapiens.
Mazières S et al.
Scientific Reports, 2025
Molecular basis of weak D expression in the Indian population and report of a novel, predominant variant RHD allele.
Fichou Y et al.
Transfusion, 2018
A D+ blood donor with a novel RHD*D-CE(5-6)-D gene variant exhibits the low-frequency antigen RH23 (D(W) ) characteristic of the partial DVa phenotype.
Lopez GH et al.
Transfusion, 2016
Partial D phenotypes and genotypes in the Chinese population.
Ye L et al.
Transfusion, 2012
DCS-1, DCS-2, and DFV share amino acid substitutions at the extracellular RhD protein vestibule.
Flegel WA et al.
Transfusion, 2008
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
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