A historical perspective on the discovery of the Kell blood group carriers
Noninvasive prenatal blood group and HPA-1a genotyping: the current European experience
The concept of “confirmatory testing” of donors for ABO and RhD
Where are we in efforts to unravel the complexity of Rh to guide transfusion decisions?
Nomenclature for red blood cell blood group alleles
Proficiency testing for blood group genotyping
External quality assessment in molecular immunohematology: the INSTAND proficiency test program
Identification of novel silent KEL alleles causing KEL:−5 (Ko) phenotype or discordance between KEL:1,−2 phenotype/ KEL*01/02 genotype
Three novel alleles in the Kell blood group system resulting in the Knull phenotype and the first in a Native American
Molecular basis of two novel and related high-prevalence antigens in the Kell blood group system, KUCI and KANT, and their serologic and spatial association with K11 and KETI
Resolution of translation start site for the human Kell glycoprotein
Expansion of the Kell blood group system: two new high-prevalence antigens and two novel K0 (Kellnull) phenotypes
Next-generation sequencing: proof of concept for antenatal prediction of the fetal Kell blood group phenotype from cell-free fetal DNA in maternal plasma
Comprehensive genotyping for 18 blood group systems using a multiplex ligation-dependent probe amplification assay shows a high degree of accuracy
Molecular genetic analysis of ABO blood group variations reveals 29 novel ABO subgroup alleles
Mutation of the GATA site in the erythroid cell–specific regulatory element of the ABO gene in a Bm subgroup individual
P1 / P2 genotyping of known and novel null alleles in the P1PK and GLOB histo-blood group systems
Combining serology and molecular typing of weak D role in improving D typing strategy in Egypt
RHD variants in Polish blood donors routinely typed as D–
Novel RHD alleles with weak hemagglutination and genetic Exon 9 diversity: weak D Types 45.1, 75, and 76
D category IV: a group of clinically relevant and phylogenetically diverse partial D
A convenient qualitative and quantitative method to investigate RHD - RHCE hybrid genes
RHCE*ceMO is frequently in cis to RHD*DAU0 and encodes a hrS–, hrB–, RH:–61 phenotype in black persons: clinical significance
Molecular background of novel silent RHCE alleles
Serologic and molecular investigations of DAR1 (weak D Type 4.2), DAR1.2, DAR1.3, DAR2 (DARE), and DARA
A comprehensive survey of both RHD and RHCE allele frequencies in sub-Saharan Africa
New RHCE variant alleles encoding the D– – phenotype
A novel JK*02 allele in a French Canadian family