Associated Papers
Frequency of RHD variants among blood donors in the central region of Iran, Yazd province.
Seddighi N et al.
Transfusion Medicine (oxford, England), 2025
Whole-exome mutational landscape of neuroendocrine carcinomas of the gallbladder.
Liu F et al.
Signal Transduction and Targeted Therapy, 2021
33563892 (PubMed )
Supplement: 41392_2020_412_MOESM7_ESM.xlsx › Supplementary_Table_S6
Overcoming the challenges of interpreting complex and uncommon RH alleles from whole genomes.
Halls JBL et al.
Vox Sanguinis, 2020
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
RHD genotype and zygosity analysis in the Chinese Southern Han D+, D- and D variant donors using the multiplex ligation-dependent probe amplification assay.
Ji YL et al.
Vox Sanguinis, 2017
RhD variants in Caucasians: consequences for checking clinically relevant alleles.
Ansart-Pirenne H et al.
Transfusion, 2004
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