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Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer)
  1. Correspondence to:
 J L Whittaker
 Department of Medical Genetics, Box 134, Addenbrooke’s Hospital, Cambridge, UK; joanne.whittakeraddenbrookes.nhs.uk
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Whittaker JL, Mattocks C, Baralle D, et al
Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer)

Publication history

  • First published July 1, 2005.
Online issue publication 
April 27, 2016

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