Associated Papers
Introduction of an Optimized Protocol for Long-Read Nanopore Sequencing of Blood Group Genes in Immunohematology Case Studies.
Wörner L et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2026
Frequency of RHD variants among blood donors in the central region of Iran, Yazd province.
Seddighi N et al.
Transfusion Medicine (oxford, England), 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
Evaluation of the LightCycler® PRO Instrument as a Platform for Rhesus D Typing.
Polin H et al.
Biomedicines, 2024
Estimating the serological underrecognition of patients with weak or partial RHD variants.
Ramsey G et al.
Transfusion, 2024
Pervasive occurrence of splice-site-creating mutations and their possible involvement in genetic disorders.
Sakaguchi N et al.
Npj Genomic Medicine, 2022
Optimization of diagnostic strategy for non-invasive cell-free foetal RHD determination from maternal plasma.
Pazourkova E et al.
Vox Sanguinis, 2021
Molecular characterization of RhD variant phenotypes among blood donors: A study from the coastal region of India.
Polavarapu I et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2021
Insights into anti-D formation in carriers of RhD variants through studies of 3D intraprotein interactions.
Floch A et al.
Transfusion, 2021
The Significance of RHD Genotyping and Characteristic Analysis in Chinese RhD Variant Individuals.
Ying Y et al.
Frontiers in Immunology, 2021
RHD Genotypes in a Chinese Cohort of Pregnant Women.
Zhang J et al.
Frontiers in Genetics, 2021
Next-generation sequencing of 35 RHD variants in 16 253 serologically D- pregnant women in the Finnish population.
Tammi SM et al.
Blood Advances, 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
A multi-centre study on the performance of the molecular genotyping platform ID RHD XT for resolving serological weak RhD phenotype in routine clinical practice.
Londero D et al.
Vox Sanguinis, 2020
Weak D type 1, 2 and 3 subtype alleles are rare in the Western French population.
Raud L et al.
Transfusion Medicine (oxford, England), 2019
Complete RHD next-generation sequencing: establishment of reference RHD alleles.
Tounsi WA et al.
Blood Advances, 2018
Performance evaluation study of ID RHD XT, a new genotyping assay for the detection of high-prevalence RhD negative and weak D types.
Molano A et al.
Vox Sanguinis, 2018
RHCE variants inherited with altered RHD alleles in Brazilian blood donors.
Prisco Arnoni C et al.
Transfusion Medicine (oxford, England), 2016
Comprehensive analysis of RHD alleles in Argentineans with variant D phenotypes.
Brajovich ME et al.
Transfusion, 2012
Overcoming methodical limits of standard RHD genotyping by next-generation sequencing.
Stabentheiner S et al.
Vox Sanguinis, 2011
Weak D and DEL alleles detected by routine SNaPshot genotyping: identification of four novel RHD alleles.
Silvy M et al.
Transfusion, 2011
[Molecular approaches to the Rh blood group system].
Kajii E
Nihon Hoigaku Zasshi = the Japanese Journal of Legal Medicine, 2006
The evolution and formation of RH genes.
Okuda H et al.
Legal Medicine (tokyo, Japan), 2002
RHD gene mutations and the weak D phenotype: an Australian blood donor study.
Cowley NM et al.
Vox Sanguinis, 2000
Advance in the Rh blood group system.
Kajii E
Nihon Hoigaku Zasshi = the Japanese Journal of Legal Medicine, 1998