Related Experiment Video
Updated: May 10, 2026

11:54
Microsatellite DNA Genotyping and Flow Cytometry Ploidy Analyses of Formalin-fixed Paraffin-embedded Hydatidiform Molar Tissues
Published on: October 20, 2019
[A KEL*02mod allele responsible for an apparent maternity exclusion]
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.
Area of Science:
- Immunology
- Genetics
- Hematology
Background:
- Routine erythrocyte typing revealed a rare KEL:1,-2 phenotype in a patient.
- The patient's daughters exhibited a KEL:-1,2 phenotype, initially suggesting maternity exclusion.
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