A combination of the effects of rare genotypes at the XK and Kel blood group loci results in absence of Kell system antigens from the red blood cells

Blood

Volumn 88, Issue 10, 1996, Pages 4045-4050

  Daniels, G L ^a   Weinauer, F ^b   Stone, C ^b   Ho, M ^b   Green, C A ^b   Jahn Jochem, H ^b   Offner, R ^b   Monaco, A P ^b  

^a NHS BLOOD AND TRANSPLANT   (United Kingdom)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ERYTHROCYTE ANTIGEN; MEMBRANE PROTEIN;

ADULT; ARTICLE; BLOOD GROUP KELL SYSTEM; BLOOD GROUP TYPING; CASE REPORT; CONTROLLED STUDY; DNA DETERMINATION; ERYTHROCYTE MEMBRANE; FEMALE; GENE LOCUS; GENE MUTATION; GENOTYPE; HUMAN; HUMAN CELL; IMMUNOBLOTTING; MALE; PEDIGREE; PHENOTYPE; POLYACRYLAMIDE GEL ELECTROPHORESIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SEROLOGY;

EID: 0029826394     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v88.10.4045.bloodjournal88104045     Document Type: Article

References (27)

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