Associated Papers
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
Missense RHD single nucleotide variants induce weakened D antigen expression by altering splicing and/or protein expression.
Raud L et al.
Transfusion, 2021
Impact of RHD genotyping on transfusion practice in Denmark and the United States and identification of novel RHD alleles.
Vege S et al.
Transfusion, 2021
RHD genotyping of serological weak D phenotypes in the Iranian blood donors and patients.
Oodi A et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2020
Transfusion strategy for weak D Type 4.0 based on RHD alleles and RH haplotypes in Tunisia.
Ouchari M et al.
Transfusion, 2018
Prevalence of RHD alleles in Japanese individuals with weak D phenotype: Identification of 20 new RHD alleles.
Isa K et al.
Vox Sanguinis, 2016
Frequency and characterization of known and novel RHD variant alleles in 37 782 Dutch D-negative pregnant women.
Stegmann TC et al.
British Journal of Haematology, 2016
Weak D alleles in Japanese: a c.960G>A silent mutation in exon 7 of the RHD gene that affects D expression.
Ogasawara K et al.
Vox Sanguinis, 2016
Variant screening of the RHD gene in a large cohort of subjects with D phenotype ambiguity: report of 17 novel rare alleles.
Fichou Y et al.
Transfusion, 2012
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