Associated Papers
Transfusion management of Africans with RHD variants in China.
Yin Q et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2023
High prevalence of weak D type 42 in a large-scale RHD genotyping program in the province of Quebec (Canada).
Leiva-Torres GA et al.
Transfusion, 2021
Insights into anti-D formation in carriers of RhD variants through studies of 3D intraprotein interactions.
Floch A et al.
Transfusion, 2021
Corrigendum: Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effort.
Leman R et al.
Nucleic Acids Research, 2018
30321405 (PubMed )
Supplement: gky979_supplemental_files.zip › Corrigendum_supplementary_table.xlsx › AllData
Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effort.
Leman R et al.
Nucleic Acids Research, 2018
29750258 (PubMed )
Supplement: gky372_supplemental_files.zip › SPiCE_table_supp.R2.xlsx › Table_S3
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
Partial D, weak D types, and novel RHD alleles among 33,864 multiethnic patients: implications for anti-D alloimmunization and prevention.
Denomme GA et al.
Transfusion, 2005
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