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Original article
Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation

Authors

  1. Correspondence to Dr Dagan Wells, University of Oxford, Department of Obstetrics and Gynaecology, John Radcliffe Hospital, Women's Centre, Oxford, OX3 9DU, UK; dagan.wells{at}obs-gyn.ox.ac.uk
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Citation

Wells D, Kaur K, Grifo J, et al
Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation

Publication history

  • Received April 29, 2014
  • Revised June 4, 2014
  • Accepted June 20, 2014
  • First published July 16, 2014.
Online issue publication 
July 16, 2014
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