Associated Papers
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
Diverse and novel RHD variants in Australian blood donors with a weak D phenotype: implication for transfusion management.
McGowan EC et al.
Vox Sanguinis, 2017
Comprehensive analysis of RHD splicing transcripts reveals the molecular basis for the weak anti-D reactivity of Del -red blood cells.
Chen DP et al.
Transfusion Medicine (oxford, England), 2016
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
Molecular RHD screening of RhD negative donors can replace standard serological testing for RhD negative donors.
Gowland P et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2014
Weak D phenotypes caused by intronic mutations in the RHD gene: four novel weak D alleles identified in the Chinese population.
Ye L et al.
Transfusion, 2013
Identification of 12 novel RHD alleles in western France by denaturing high-performance liquid chromatography analysis.
Le Maréchal C et al.
Transfusion, 2007
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