Associated Papers
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
40 years of researching the Del phenotype results in a change of transfusion practice.
Flegel WA et al.
Transfusion, 2024
DEL variants: review of molecular mechanisms, clinical consequences and molecular testing strategy.
Yin Q
Functional & Integrative Genomics, 2023
Transfusion management of Africans with RHD variants in China.
Yin Q et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2023
Genotype analysis to clarify RhD variants in discrepant samples of Chilean population.
Aburto A et al.
Frontiers in Immunology, 2023
Single-exon approach to non-invasive fetal RHD screening in early pregnancy: An update after 10 years' experience.
Uzunel M et al.
Vox Sanguinis, 2022
Rh Blood Group D Antigen Genotyping Using a Portable Nanopore-based Sequencing Device: Proof of Principle.
Tounsi WA et al.
Clinical Chemistry, 2022
Insights into anti-D formation in carriers of RhD variants through studies of 3D intraprotein interactions.
Floch A et al.
Transfusion, 2021
D variants in the population of D-negative blood donors in the north-eastern region of Croatia.
Safic Stanic H et al.
Transfusion Medicine (oxford, England), 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
RHD Genotyping by Molecular Analysis of Hybrid Rhesus box in RhD-Negative Blood Donors from Iran.
Khosroshahi BN et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion, 2019
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
Screening for DEL phenotype in RhD negative Indians.
Kulkarni S et al.
Journal of Clinical Laboratory Analysis, 2018
Evaluation of the applicability and effectiveness of a molecular strategy for identifying weak D and DEL phenotype among D- blood donors of mixed origin exhibiting high frequency of RHD*Ψ.
Dezan MR et al.
Transfusion, 2018
Application of Multiplex Ligation-Dependent Probe Amplification Assay for Genotyping Major Blood Group Systems Including DEL Variants in the D-Negative Korean Population.
Kim B et al.
Annals of Laboratory Medicine, 2018
RHD-specific microRNA for regulation of the DEL blood group: integration of computational and experimental approaches.
Thongbut J et al.
British Journal of Biomedical Science, 2017
Diverse and novel RHD variants in Australian blood donors with a weak D phenotype: implication for transfusion management.
McGowan EC et al.
Vox Sanguinis, 2017
Prevalence of RhD status and clinical application of non-invasive prenatal determination of fetal RHD in maternal plasma: a 5 year experience in Cyprus.
Papasavva T et al.
Bmc Research Notes, 2016
Comprehensive analysis of RHD splicing transcripts reveals the molecular basis for the weak anti-D reactivity of Del -red blood cells.
Chen DP et al.
Transfusion Medicine (oxford, England), 2016
Molecular basis for D- Japanese: identification of novel DEL and D- alleles.
Ogasawara K et al.
Vox Sanguinis, 2015
Prospective Evaluation of a Transfusion Policy of RhD-Positive Red Blood Cells into DEL Patients in China.
Xu W et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2015
The RHD(1227G>A) DEL-associated allele is the most prevalent DEL allele in Australian D- blood donors with C+ and/or E+ phenotypes.
Scott SA et al.
Transfusion, 2014
Molecular structures identified in serologically D- samples of an admixed population.
Trucco Boggione C et al.
Transfusion, 2014
Characteristics and frequency of DEL phenotype detected by indirect antiglobulin test in Dalmatia county of Croatia.
Dajak S et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2014
Molecular RHD screening of RhD negative donors can replace standard serological testing for RhD negative donors.
Gowland P et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2014
Systematic RH genotyping and variant identification in French donors of African origin.
Kappler-Gratias S et al.
Blood Transfusion = Trasfusione Del Sangue, 2014
Clinical and laboratory update on the DEL variant.
Nuchnoi P et al.
Laboratory Medicine, 2014
Blood group genotyping in multi-transfused patients.
Bakanay SM et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2013
Molecular background of D-negative phenotype in the Tunisian population.
Moussa H et al.
Transfusion Medicine (oxford, England), 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
Antenatal Rh prophylaxis is unnecessary for "Asia type" DEL women.
Shao CP et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2010
[Genotyping of 21,000 blood donors in Quebec and RHD analysis].
St-Louis M et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2010
Molecular basis of the RHD gene in blood donors with DEL phenotypes in Shanghai.
Li Q et al.
Vox Sanguinis, 2009
Primary anti-D immunization by DEL red blood cells.
Kim KH et al.
The Korean Journal of Laboratory Medicine, 2009
Identification of RHD alleles with the potential of anti-D immunization among seemingly D- blood donors in Upper Austria.
Polin H et al.
Transfusion, 2009
Six years' experience performing RHD genotyping to confirm D- red blood cell units in Germany for preventing anti-D immunizations.
Flegel WA et al.
Transfusion, 2009
Molecular basis of D variants between Uigur and Han blood donors in Xinjiang.
Li Q et al.
Transfusion Medicine (oxford, England), 2008
The structure and function of the Rh antigen complex.
Westhoff CM
Seminars in Hematology, 2007
An easy RHD genotyping strategy for D- East Asian persons applied to Korean blood donors.
Luettringhaus TA et al.
Transfusion, 2006
[Molecular approaches to the Rh blood group system].
Kajii E
Nihon Hoigaku Zasshi = the Japanese Journal of Legal Medicine, 2006
A comprehensive analysis of DEL types: partial DEL individuals are prone to anti-D alloimmunization.
Körmöczi GF et al.
Transfusion, 2005
Novel weak D types 31 and 32: adsorption-elution-supported D antigen analysis and comparison to prevalent weak D types.
Körmöczi GF et al.
Transfusion, 2005
Secondary anti-D immunization by Del red blood cells.
Yasuda H et al.
Transfusion, 2005
Random survey for RHD alleles among D+ European persons.
Chen Q et al.
Transfusion, 2005
Presence of RHD in serologically D-, C/E+ individuals: a European multicenter study.
Gassner C et al.
Transfusion, 2005
The evolution and formation of RH genes.
Okuda H et al.
Legal Medicine (tokyo, Japan), 2002
RHD positive haplotypes in D negative Europeans.
Wagner FF et al.
Bmc Genetics, 2001