Associated Papers
A new RhD variant allele is caused by a RhD 26 T > G mutation in a Chinese Han woman with a weak D phenotype.
Qian C et al.
Transfusion, 2019
Novel weak D types 31 and 32: adsorption-elution-supported D antigen analysis and comparison to prevalent weak D types.
Körmöczi GF et al.
Transfusion, 2005
Presence of RHD in serologically D-, C/E+ individuals: a European multicenter study.
Gassner C et al.
Transfusion, 2005
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