Associated Papers
Combining computational approaches and functional analysis for characterizing the deleterious effect of RHD gene variants on splicing in the Chinese population.
Jia S et al.
Transfusion, 2025
RHD alleles contributing to serologically weak D phenotypes in China: A single-centre study over 10 years.
Ye L et al.
Vox Sanguinis, 2022
[Molecular genetic analysis of two individuals with weak D variant of the Rh blood type].
He Y et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2021
The Significance of RHD Genotyping and Characteristic Analysis in Chinese RhD Variant Individuals.
Ying Y et al.
Frontiers in Immunology, 2021
A new RHD variant allele in Exon 2 identified in a Chinese individual.
Zhu Y et al.
Transfusion, 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
Prevalence of RHD alleles in Japanese individuals with weak D phenotype: Identification of 20 new RHD alleles.
Isa K et al.
Vox Sanguinis, 2016
Variant screening of the RHD gene in a large cohort of subjects with D phenotype ambiguity: report of 17 novel rare alleles.
Fichou Y et al.
Transfusion, 2012
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