Associated Papers
First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central Africa.
Mbeti JMM et al.
Blood Transfusion = Trasfusione Del Sangue, 2024
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
The Significance of RHD Genotyping and Characteristic Analysis in Chinese RhD Variant Individuals.
Ying Y et al.
Frontiers in Immunology, 2021
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
Prevalence of RHD alleles in Japanese individuals with weak D phenotype: Identification of 20 new RHD alleles.
Isa K et al.
Vox Sanguinis, 2016
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
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
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
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
Transcript analysis of D category phenotypes predicts hybrid Rh D-CE-D proteins associated with alteration of D epitopes.
Rouillac C et al.
Blood, 1995
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