Associated Papers
Partial D variant with demonstrated risk of D alloimmunization in the Australian Indigenous population.
Palfreyman E et al.
Vox Sanguinis, 2025
Alloanti-D induction in a rare RhD variant (DBT-2) case: Insights from serological and molecular biological testing.
Xu Z et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2025
Rapid change in red cell blood group systems after the main Out of Africa of Homo sapiens.
Mazières S et al.
Scientific Reports, 2025
Single-exon fetal RHD genotyping: a 31-month follow up in the obstetric population of Western Sweden.
Pardi C et al.
Blood Transfusion = Trasfusione Del Sangue, 2024
Machine learning to optimize automated RH genotyping using whole-exome sequencing data.
Chang TC et al.
Blood Advances, 2024
RHD Genotyping of Rh-Negative and Weak D Phenotype among Blood Donors in Southeast Iran.
Sadeghi-Bojd Y et al.
International Journal of Hematology-oncology and Stem Cell Research, 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
Classification of major and minor blood group antigens in the Kuwaiti Arab population.
Ameen R et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2020
Genomic characterization of the RH locus detects complex and novel structural variation in multi-ethnic cohorts.
Wheeler MM et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
Molecular basis of weak D expression in the Indian population and report of a novel, predominant variant RHD allele.
Fichou Y et al.
Transfusion, 2018
A D+ blood donor with a novel RHD*D-CE(5-6)-D gene variant exhibits the low-frequency antigen RH23 (D(W) ) characteristic of the partial DVa phenotype.
Lopez GH et al.
Transfusion, 2016
Partial D phenotypes and genotypes in the Chinese population.
Ye L et al.
Transfusion, 2012
DCS-1, DCS-2, and DFV share amino acid substitutions at the extracellular RhD protein vestibule.
Flegel WA et al.
Transfusion, 2008
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
Random survey for RHD alleles among D+ European persons.
Chen Q et al.
Transfusion, 2005
A D(V)-like phenotype is obliterated by A226P in the partial D DBS.
Wagner FF et al.
Transfusion, 2001
PCR screening for common weak D types shows different distributions in three Central European populations.
Müller TH et al.
Transfusion, 2001