Associated Papers
Molecular Basis of KELnull Phenotype in Brazilians.
Boturão-Neto E et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2015
Identification of novel silent KEL alleles causing KEL:-5 (Ko) phenotype or discordance between KEL:1,-2 phenotype/KEL*01/02 genotype.
Martin-Blanc S et al.
Transfusion, 2013
Genetic diversity of KELnull and KELel: a nationwide Austrian survey.
Körmöczi GF et al.
Transfusion, 2007
Select a paper to view details