Associated Papers
Risk Minimization of Hemolytic Disease of the Fetus and Newborn Using Droplet Digital PCR Method for Accurate Fetal Genotype Assessment of RHD, KEL, and RHCE from Cell-Free Fetal DNA of Maternal Plasma.
Vodicka R et al.
Diagnostics (basel, Switzerland), 2021
Impact of RHD genotyping on transfusion practice in Denmark and the United States and identification of novel RHD alleles.
Vege S et al.
Transfusion, 2021
RHD-Positive Alleles among D- C/E+ Individuals from India.
Kulkarni SS et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2018
Serologic and molecular characterization of weak D type 29.
Ouchari M et al.
Transfusion, 2017
RH diversity in Mali: characterization of a new haplotype RHD*DIVa/RHCE*ceTI(D2).
Ba A et al.
Transfusion, 2015
A comprehensive survey of both RHD and RHCE allele frequencies in sub-Saharan Africa.
Granier T et al.
Transfusion, 2013
RHD and RHCE variant and zygosity genotyping via multiplex ligation-dependent probe amplification.
Haer-Wigman L et al.
Transfusion, 2013
DIII Type 7 is likely the original serologically defined DIIIb.
Lomas-Francis C et al.
Transfusion, 2012
Molecular analysis of blood group Rh transcripts from a rGr variant.
Mouro I et al.
British Journal of Haematology, 1996
Molecular analysis of selected Rh variants.
Noizat-Pirenne F et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 1996
Lack of G blood group antigen in DIIIb erythrocytes is associated with segmental DNA exchange between RH genes.
Rouillac C et al.
British Journal of Haematology, 1995
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