[A KEL*02mod allele responsible for an apparent maternity exclusion]

M Monfort1, T Peyrard, L Arnaud

  • 1Laboratoire d'immunohématologie, centre hospitalier universitaire de Liège, Liège, Belgique.

Summary

A rare KEL blood group phenotype was identified in a patient, initially suggesting maternity exclusion with her daughters. Further analysis revealed a weak KEL2 expression, clarifying the genetic discrepancy.

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