Associated Papers
RHD alleles contributing to serologically weak D phenotypes in China: A single-centre study over 10 years.
Ye L et al.
Vox Sanguinis, 2022
A novel double-variant RHAG allele leads to Rhmod phenotype.
Xia RW et al.
Transfusion Medicine (oxford, England), 2019
The synonymous nucleotide substitution RHD 1056C>G alters mRNA splicing associated with serologically weak D phenotype.
Chun S et al.
Journal of Clinical Laboratory Analysis, 2018
Extensive functional analyses of RHD splice site variants: Insights into the potential role of splicing in the physiology of Rh.
Fichou Y et al.
Transfusion, 2015
A comprehensive investigation of RHD polymorphisms in the Chinese Han population in Xi'an.
Ye SH et al.
Blood Transfusion = Trasfusione Del Sangue, 2014
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