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Justification of direct Sanger sequencing application for detection of KIT and PDGFRα gene mutations in formalin-fixed, paraffin-embedded samples from gastrointestinal stromal tumours

Authors

  • Katarzyna Kiwerska Department of Tumor Pathology, Greater Poland Cancer Centre, Poznan, Poland Institute of Human Genetics, Polish Academy of Sciences, Poznan, Poland PubMed articlesGoogle scholar articles
  • Joanna Wroblewska Department of Tumor Pathology and Prophylaxis, Poznan University of Medical Sciences & Greater Poland Cancer Centre, Poznan, Poland PubMed articlesGoogle scholar articles
  • Apolonia Kaluzna Department of Tumor Pathology and Prophylaxis, Poznan University of Medical Sciences & Greater Poland Cancer Centre, Poznan, Poland PubMed articlesGoogle scholar articles
  • Andrzej Marszalek Department of Tumor Pathology and Prophylaxis, Poznan University of Medical Sciences & Greater Poland Cancer Centre, Poznan, Poland PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Katarzyna Kiwerska, Department of Tumor Pathology, Greater Poland Cancer Centre, Poznan 61-866, Poland; katarzyna.kiwerska{at}wco.pl
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Citation

Kiwerska K, Wroblewska J, Kaluzna A, et al
Justification of direct Sanger sequencing application for detection of KIT and PDGFRα gene mutations in formalin-fixed, paraffin-embedded samples from gastrointestinal stromal tumours

Publication history

  • Received September 20, 2019
  • Revised October 1, 2019
  • Accepted October 2, 2019
  • First published October 24, 2019.
Online issue publication 
March 20, 2020

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