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Article

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

Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine - 1 Dec 2013

Monfort M, Peyrard T, Arnaud L, Helias V, Maggipinto G, Gérard C

Abstract excerpt

The patient's rare KEL:1,-2 phenotype was highlighted in course of a routine preoperative erythrocyte typing. Unexpectedly, her two daughters presented a KEL:-1,2 phenotype what appeared first as an apparent maternity exclusion. Flow cytometry, genotyping and adsorption-elution analyses were then performed for those three patients. KEL genotyping showed that the patient's genotype was KEL*01/KEL*02 whereas that...

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Source

Identifiers

PMID: 23727116
DOI: 10.1016/j.tracli.2013.03.278

Genes

KEL

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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