Associated Papers
[Serological and Molecular Biological Detection of RhD Variants].
Ren DJ et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi, 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
Molecular and serological analysis of the D variant in the Chinese population and identification of seven novel RHD alleles.
Wen J et al.
Transfusion, 2023
RHD alleles contributing to serologically weak D phenotypes in China: A single-centre study over 10 years.
Ye L et al.
Vox Sanguinis, 2022
The synonymous nucleotide substitution RHD 1056C>G alters mRNA splicing associated with serologically weak D phenotype.
Chun S et al.
Journal of Clinical Laboratory Analysis, 2018
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
The Duffy blood group system in the Tunisian population.
Ouchari M et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2015
Genomic analyses of RH alleles to improve transfusion therapy in patients with sickle cell disease.
Reid ME et al.
Blood Cells, Molecules & Diseases, 2014
Overcoming methodical limits of standard RHD genotyping by next-generation sequencing.
Stabentheiner S et al.
Vox Sanguinis, 2011
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