Associated Papers
A cold case of hemolytic disease of the fetus and newborn resolved by genomic sequencing and population studies to define a new antigen in the Rh system.
Wilson B et al.
Transfusion, 2024
RHCE*cE734C allele encodes an altered c antigen and a suppressed E antigen not detected with standard reagents.
Silvy M et al.
Transfusion, 2013
Analysis of RhCE variants among 806 individuals in France: considerations for transfusion safety, with emphasis on patients with sickle cell disease.
Pham BN et al.
Transfusion, 2011
A novel RHCE*ce 48C, 733G allele with Nucleotide 941C in Exon 7 encodes an altered red blood cell e antigen.
Hue-Roye K et al.
Transfusion, 2011
The low prevalence Rh antigen Be(a) (Rh36) is associated with RHCE*ce 662C>G in exon 5, which is predicted to encode Rhce 221Arg.
Hue-Roye K et al.
Vox Sanguinis, 2010
RHCE alleles detected after weak and/or discrepant results in automated Rh blood grouping of blood donors in Northern Germany.
Döscher A et al.
Transfusion, 2009
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