Unusual association of three rare alleles and a mismatch in a case of paternity testing
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Updated: Aug 25, 2026

Microsatellite DNA Genotyping and Flow Cytometry Ploidy Analyses of Formalin-fixed Paraffin-embedded Hydatidiform Molar Tissues
Published on: October 20, 2019
Chiara Turchi1, Mauro Pesaresi, Federica Alessandrini
1Istituto di Medicina Legale, Universita di Ancona, Policlinico Torrette, 1-60020 Ancona, Italy.
Abstract:
This study reports a paternity case analyzed by the AmpFlSTR Identifiler Kit (AB) in which father and daughter shared three rare alleles for D19S433, D18S51 and TH01 microsatellites. The case also showed an apparent exclusion, due to a mutation at the D3S 1358 microsatellite. Sequencing analysis was performed to assess the size of the rare alleles and to establish their structure, which revealed some molecular variations in regions flanking the motif repeats.
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