Associated Papers
A serologic weak D caused by a novel RHD allele with single nucleotide c.209G>C variation predicted to encode p.Arg70Pro.
Heng E et al.
Transfusion, 2025
Combining computational approaches and functional analysis for characterizing the deleterious effect of RHD gene variants on splicing in the Chinese population.
Jia S et al.
Transfusion, 2025
The Significance of RHD Genotyping and Characteristic Analysis in Chinese RhD Variant Individuals.
Ying Y et al.
Frontiers in Immunology, 2021
D category IV: a group of clinically relevant and phylogenetically diverse partial D.
von Zabern I et al.
Transfusion, 2013
D variants at the RhD vestibule in the weak D type 4 and Eurasian D clusters.
Flegel WA et al.
Transfusion, 2009
RHD(T201R, F223V) cluster analysis in five different ethnic groups and serologic characterization of a new Ethiopian variant DARE, the DIII type 6, and the RHD(F223V).
Grootkerk-Tax MG et al.
Transfusion, 2006
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