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 place of work:
Ústav biologie a lékařské genetiky, 2. LF UK a FN v Motole, Praha
1; Klinika plastické chirurgie, Nemocnice Na Bulovce, Praha
2
Published in the journal:
Klin Onkol 2014; 27(4): 303
Category:
Oncology in Images
Summary
Submitted:
25. 7. 2014
Zdroje
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.
Štítky
Paediatric clinical oncology Surgery Clinical oncologyČlánok vyšiel v časopise
Clinical Oncology
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