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Case report
Delineation of an unknown significance FANCA genetic variant in a recurrent breast cancer patient

Authors

  • Stavroula Kastora Acute Medicine, Grampian University Hospitals NHS Trust, Aberdeen, UKSchool of Medicine, University of Aberdeen College of Life Sciences & Medicine, Aberdeen, UK PubMed articlesGoogle scholar articles
  • Olga Triantafyllidou Reproductive Medicine Unit, “Leto” Maternity Hospital, Athens, Greece2nd Department of Obstetrics and Gynaecology, Aretaieion Panepistemiako Nosokomeio, Athens, Attica, Greece PubMed articlesGoogle scholar articles
  • Georgios Kounidas School of Medicine, University of Aberdeen College of Life Sciences & Medicine, Aberdeen, UK PubMed articlesGoogle scholar articles
  • Nikolaos Vlahos 2nd Department of Obstetrics and Gynaecology, Aretaieion Panepistemiako Nosokomeio, Athens, Attica, Greece PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Stavroula Kastora; stavroula.kastora{at}abdn.ac.uk
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Citation

Kastora S, Triantafyllidou O, Kounidas G, et al
Delineation of an unknown significance FANCA genetic variant in a recurrent breast cancer patient
BMJ Case Reports CP 2021;14:e241251.

Publication history

  • Accepted March 2, 2021
  • First published March 24, 2021.
Online issue publication 
January 24, 2024

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© BMJ Publishing Group Limited 2021. No commercial re-use. See rights and permissions. Published by BMJ.