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
Alloanti-D induction in a rare RhD variant (DBT-2) case: Insights from serological and molecular biological testing.
Xu Z et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2025
Machine learning to optimize automated RH genotyping using whole-exome sequencing data.
Chang TC et al.
Blood Advances, 2024
38522094 (PubMed )
Supplement: BLOODA_ADV-2023-011660-mmc1.xlsx › Rh__2_
Benchmarking of Whole Exome Sequencing and Ad Hoc Designed Panels for Genetic Testing of Hereditary Cancer.
Feliubadaló L et al.
Scientific Reports, 2017
28050010 (PubMed )
Supplement: srep37984-s2.xls › Exome_geMODERATE_variants
How do we identify RHD variants using a practical molecular approach?
Arnoni CP et al.
Transfusion, 2014
Novel RHD alleles with weak hemagglutination and genetic Exon 9 diversity: weak D Types 45.1, 75, and 76.
Gassner C et al.
Transfusion, 2013
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
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
Evidence for a separate genetic origin of the partial D phenotype DBT in a Japanese family.
Huang CH et al.
Transfusion, 0
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