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Incidental detection of germline variants of potential clinical significance by massively parallel sequencing in haematological malignancies

Authors

  1. Correspondence to Dr Costas K Yannakou, Department of Molecular Haematology, Pathology – Level 4, Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne VIC 3000, Australia; costas.yannakou{at}petermac.org
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Citation

Yannakou CK, Jones K, Ryland GL, et al
Incidental detection of germline variants of potential clinical significance by massively parallel sequencing in haematological malignancies

Publication history

  • Received March 28, 2017
  • Revised July 14, 2017
  • Accepted July 19, 2017
  • First published August 11, 2017.
Online issue publication 
September 21, 2020

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