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Pacient s Cowdenovým syndromem způsobeným mutací v genu PTEN (archiv 2. LF UK a FN v Motole)


Authors: A. Puchmajerová 1;  P. Vasovčák 1;  V. Poláček 2
Authors‘ workplace: Ústav bio­logie a lékařské genetiky, 2. LF UK a FN v Motole, Praha 1;  Klinika plastické chirurgie, Nemocnice Na Bulovce, Praha 2
Published in: Klin Onkol 2014; 27(4): 303
Category: Oncology in Images

Overview

Submitted:
25. 7. 2014


Sources

1. Vasovcak P, Krepelova A, Puchmajerova A et al. A novel mutation of PTEN gene in a patient with Cowden synd­rome with excessive papillomatosis of the lips, discrete cutaneous lesions, and gastrointestinal polyposis. Eur J Gastroenterol Hepatol 2007; 19(6): 513–517.

2. Puchmajerová A, Vasovčák P, Křepelová A et al. Cowdenův syndrom. Klin Onkol 2009; 22 (Suppl): S56– S57.

Labels
Paediatric clinical oncology Surgery Clinical oncology

Article was published in

Clinical Oncology

Issue 4

2014 Issue 4

Most read in this issue
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