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Two distinct thyroid tumours in a patient with Cowden syndrome carrying both a 10q23 and a mitochondrial DNA germline deletion
  1. Correspondence to Dr Daniela Turchetti, Cattedra e U.O. Genetica Medica, Dipartimento di Scienze Ginecologiche, Ostetriche e Pediatriche, Policlinico Sant'Orsola-Malpighi, Padiglione 11, via Massarenti, 9, 40138 Bologna, Italy; daniela.turchetti{at}unibo.it
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Pradella LM, Zuntini R, Magini P, et al
Two distinct thyroid tumours in a patient with Cowden syndrome carrying both a 10q23 and a mitochondrial DNA germline deletion

Publication history

  • Received April 29, 2011
  • Revised August 5, 2011
  • Accepted August 15, 2011
  • First published September 16, 2011.
Online issue publication 
April 27, 2016

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