Associated Papers
Molecular Blood Group Screening in Donors from Arabian Countries and Iran Using High-Throughput MALDI-TOF Mass Spectrometry and PCR-SSP.
Flesch BK et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2020
A novel algorithm comprehensively characterizes human RH genes using whole-genome sequencing data.
Chang TC et al.
Blood Advances, 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
Next-Generation Sequencing Technologies in Blood Group Typing.
Fürst D 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 study of Cw /Cx antigens and frequency of Rh phenotypes in southeast Brazilian blood donors.
Costa SS et al.
Journal of Clinical Laboratory Analysis, 2018
Evaluation of targeted exome sequencing for 28 protein-based blood group systems, including the homologous gene systems, for blood group genotyping.
Schoeman EM et al.
Transfusion, 2017
Genotyping of 28 blood group alleles in blood donors from Mali: Prediction of rare phenotypes.
Ba A et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2016
A simple genotyping procedure without DNA extraction to identify rare blood donors.
Silvy M et al.
Vox Sanguinis, 2015
Integrated analysis of germline and somatic variants in ovarian cancer.
Kanchi KL et al.
Nature Communications, 2014
A G613A missense in the Hutchinson's progeria lamin A/C gene causes a lone, autosomal dominant atrioventricular block.
Villa F et al.
Immunity & Ageing : I & A, 2014
RHCE alleles detected after weak and/or discrepant results in automated Rh blood grouping of blood donors in Northern Germany.
Döscher A et al.
Transfusion, 2009
RhCE protein variants in Southwestern Germany detected by serologic routine testing.
Bugert P et al.
Transfusion, 2009
[Molecular approaches to the Rh blood group system].
Kajii E
Nihon Hoigaku Zasshi = the Japanese Journal of Legal Medicine, 2006
A new hybrid RHCE gene (CeNR) is responsible for expression of a novel antigen.
Westhoff CM et al.
Transfusion, 2004
The evolution and formation of RH genes.
Okuda H et al.
Legal Medicine (tokyo, Japan), 2002
Advance in the Rh blood group system.
Kajii E
Nihon Hoigaku Zasshi = the Japanese Journal of Legal Medicine, 1998
Molecular analysis of selected Rh variants.
Noizat-Pirenne F et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 1996
Molecular basis of the RhCW (Rh8) and RhCX (Rh9) blood group specificities.
Mouro I et al.
Blood, 1995
Hydrophobic cluster analysis and modeling of the human Rh protein three-dimensional structures.
Callebaut I et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 0