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References from A distinctive RhD serologic phenotype expressed by p. Glu233Lys RHD alleles DV type 5 and DAU4 in microplate agglutination RhD typing. Local targets link to admitted publications; unresolved targets remain external evidence.
Identification of RHD allelic variants discovered by atypical typing results on the NEO/Echo platforms
10.21307/immunohematology-2021-027 · 2021 · External reference
RHD genotyping to resolve weak and discrepant RhD patient phenotypes
10.1111/trf.17145 · 2022 · External reference
Updated evaluation of RhD status among women of child‐bearing age in Detroit, Michigan
10.1093/ajcp/aqab061 · 2021 · External reference
Strategies to identify candidates for D variant genotyping
2018 · External reference
Clinical and cost efficacy of molecular RhD genotyping
2018 · External reference
The Rh blood group system: RHD update
10.2478/immunohematology-2025-007 · 2025 · External reference
It's time to phase out “serologic weak D phenotype” and resolve D types with RHD genotyping including weak D type 4
10.1111/trf.15741 · 2020 · External reference
Impact of RHD genotyping on transfusion practice in Denmark and the United States and identification of novel RHD alleles
10.1111/trf.16100 · 2021 · External reference
RH genetic variation and the impact for typing and personalized transfusion strategies: a narrative review
10.21037/aob-22-6 · 2023 · External reference
Rh serology‐coordinator's report
10.1016/s1246-7820(96)80040-1 · 1996 · External reference
Section 1A: Rh serology coordinator's report
10.1016/s1246-7820(01)00211-7 · 2002 · External reference
Weak or discrepant RhD phenotypes: laboratory management strategies for local patient populations
10.1111/trf.17796 · 2024 · External reference
A review of the literature organized into a new database: RHeference
10.1016/j.tmrv.2021.04.002 · 2021 · External reference
Estimating the serological underrecognition of patients with weak or partial RHD variants
10.1111/trf.17810 · 2024 · External reference
The genomic organization of the partial D category DVa: the presence of a new partial D associated with the DVa phenotype
10.1006/bbrc.1998.0121 · 1999 · External reference
Detection of Rh23 in the partial D phenotype associated with the DVa category
10.1046/j.1537-2995.2000.40020256.x · 2000 · External reference
Polymorphisms of RhDVa and a new RhDVa‐like variant found in Japanese individuals
10.1046/j.1423-0410.2000.7820122.x · 2000 · External reference
Partial D phenotypes and genotypes in the Chinese population
10.1111/j.1537-2995.2011.03266.x · 2012 · External reference
RHD genotype and zygosity analysis in the Chinese southern Han D+, D‐ and D variant donors using the multiplex ligation‐dependent probe amplification assay
10.1111/vox.12554 · 2017 · External reference
RHD genotyping of serological weak D phenotypes in the Iranian blood donors and patients
10.1016/j.transci.2020.102870 · 2020 · External reference
Anti‐D antibodies in pregnant D variant antigen carriers initially typed as RhD+
10.1159/000446816 · 2016 · External reference
Frequency distribution of RHD alleles among Greek donors with weak D phenotypes demonstrates a distinct pattern in central European countries
10.1111/tme.12623 · 2019 · External reference
Anti‐D reagents should be chosen accordingly to the prevalence of D variants in the obstetric population
10.1002/jcla.22285 · 2018 · External reference
Effective molecular RHD typing strategy for blood donations
10.1111/j.1537-2995.2007.01278.x · 2007 · External reference
Single‐exon fetal RHD genotyping: a 31‐month follow up in the obstetric population of Western Sweden
2024 · External reference
Partial D, weak D types, and novel RHD alleles among 33,864 multiethnic patients: implications for anti‐D alloimmunization and prevention
10.1111/j.1537-2995.2005.00586.x · 2005 · External reference
Resolving variable maternal D typing using serology and genotyping in selected prenatal patients
10.1111/trf.13798 · 2016 · External reference
Diverse and novel RHD variants in Australian blood donors with a weak D phenotype: implication for transfusion management
10.1111/vox.12488 · 2017 · External reference
Unresolved reference
External reference
The DAU allele cluster of the RHD gene
10.1182/blood-2002-01-0320 · 2002 · External reference
Unresolved reference
External reference
A genomic mutational constraint map using variation in 76,156 human genomes
10.1038/s41586-023-06045-0 · 2024 · External reference
Insights into anti‐D formation in carriers of RhD variants through studies of 3D intraprotein interactions
10.1111/trf.16301 · 2021 · External reference
Severe hemolytic transfusion reaction due to anti‐D in a D+ patient with sickle cell disease
10.1097/mph.0000000000000241 · 2015 · External reference
10.1002/9781118493595
10.1002/9781118493595 · 2013 · External reference
The rhesus site
10.1159/000366176 · 2014 · External reference
Molecular biology of partial D and weak D: implications for blood bank practice
2002 · External reference
Reactivity of FDA‐approved anti‐D reagents with partial D red blood cells
10.21307/immunohematology-2019-409 · 2005 · External reference
D category IV: a group of clinically relevant and phylogenetically diverse partial D
10.1111/trf.12145 · 2013 · External reference
Serological weak D phenotypes: a review and guidance for interpreting the RhD blood type using the RHD genotype
10.1111/bjh.14757 · 2017 · External reference
Frequency and characterization of RHD variant alleles in a population of blood donors from southeastern Brazil: comparison with other populations
10.1016/j.transci.2021.103135 · 2021 · External reference
A DV‐like phenotype is obliterated by A226P in the partial D DBS
10.1046/j.1537-2995.2001.41081052.x · 2001 · External reference
