Associated Papers
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
First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central Africa.
Mbeti JMM et al.
Blood Transfusion = Trasfusione Del Sangue, 2024
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
Machine learning to optimize automated RH genotyping using whole-exome sequencing data.
Chang TC et al.
Blood Advances, 2024
DNA Reference Reagents for Genotyping RH Variants.
Sippert E et al.
The Journal of Molecular Diagnostics : Jmd, 2024
Transfusion support for a patient with alloanti-D and the RHD*DV.1 allele.
Jiang L et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2023
Insights into anti-D formation in carriers of RhD variants through studies of 3D intraprotein interactions.
Floch A et al.
Transfusion, 2021
A Review of the Literature Organized Into a New Database: RHeference.
Floch A et al.
Transfusion Medicine Reviews, 2021
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
Classification of major and minor blood group antigens in the Kuwaiti Arab population.
Ameen R et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2020
Comprehensive Molecular Analysis of Serologically D-Negative and Weak/Partial D Phenotype in Thai Blood Donors.
Thongbut J et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2020
Validated Reference Panel from Renewable Source of Genomic DNA Available for Standardization of Blood Group Genotyping.
Volkova E et al.
The Journal of Molecular Diagnostics : Jmd, 2019
Genomic characterization of the RH locus detects complex and novel structural variation in multi-ethnic cohorts.
Wheeler MM et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 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
Whole-exome sequencing for RH genotyping and alloimmunization risk in children with sickle cell anemia.
Chou ST et al.
Blood Advances, 2017
The DAU cluster: a comparative analysis of 18 RHD alleles, some forming partial D antigens.
Srivastava K et al.
Transfusion, 2016
A D+ blood donor with a novel RHD*D-CE(5-6)-D gene variant exhibits the low-frequency antigen RH23 (D(W) ) characteristic of the partial DVa phenotype.
Lopez GH et al.
Transfusion, 2016
A comprehensive investigation of RHD polymorphisms in the Chinese Han population in Xi'an.
Ye SH et al.
Blood Transfusion = Trasfusione Del Sangue, 2014
RHCE*ceMO is frequently in cis to RHD*DAU0 and encodes a hr(S) -, hr(B) -, RH:-61 phenotype in black persons: clinical significance.
Westhoff CM et al.
Transfusion, 2013
Serologic and molecular investigations of DAR1 (weak D Type 4.2), DAR1.2, DAR1.3, DAR2 (DARE), and DARA.
Lejon Crottet S et al.
Transfusion, 2013
Variants of RhD--current testing and clinical consequences.
Daniels G
British Journal of Haematology, 2013
Partial D phenotypes and genotypes in the Chinese population.
Ye L et al.
Transfusion, 2012
Comprehensive analysis of RHD alleles in Argentineans with variant D phenotypes.
Brajovich ME et al.
Transfusion, 2012
DIIIa and DIII Type 5 are encoded by the same allele and are associated with altered RHCE*ce alleles: clinical implications.
Westhoff CM et al.
Transfusion, 2010
Molecular analysis of inactive and active RHD alleles in native Congolese cohorts.
Touinssi M et al.
Transfusion, 2009
D variants at the RhD vestibule in the weak D type 4 and Eurasian D clusters.
Flegel WA et al.
Transfusion, 2009
DCS-1, DCS-2, and DFV share amino acid substitutions at the extracellular RhD protein vestibule.
Flegel WA et al.
Transfusion, 2008
Identification of 12 novel RHD alleles in western France by denaturing high-performance liquid chromatography analysis.
Le Maréchal C et al.
Transfusion, 2007
RHD(T201R, F223V) cluster analysis in five different ethnic groups and serologic characterization of a new Ethiopian variant DARE, the DIII type 6, and the RHD(F223V).
Grootkerk-Tax MG et al.
Transfusion, 2006
Partial D, weak D types, and novel RHD alleles among 33,864 multiethnic patients: implications for anti-D alloimmunization and prevention.
Denomme GA et al.
Transfusion, 2005
Random survey for RHD alleles among D+ European persons.
Chen Q et al.
Transfusion, 2005
PCR screening for common weak D types shows different distributions in three Central European populations.
Müller TH et al.
Transfusion, 2001
Polymorphisms of RhD(Va) and a new RhD(Va)-like variant found in Japanese individuals.
Hyodo H et al.
Vox Sanguinis, 2000
RHD genotyping in weak D phenotypes by multiple polymerase chain reactions.
Legler TJ et al.
Transfusion, 1998
[Rh-D genotyping for exon 2, 5 and 7 of German and Japanese blood donors with sequence specific polymerase chain reaction].
Maas JH et al.
Beitrage Zur Infusionstherapie Und Transfusionsmedizin = Contributions to Infusion Therapy and Transfusion Medicine, 1997
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