Article info
Cancer genetics
Short report
Two distinct thyroid tumours in a patient with Cowden syndrome carrying both a 10q23 and a mitochondrial DNA germline deletion
- 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
Citation
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
October 20, 2011
Article Versions
- Previous version (16 September 2011).
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© 2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.