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Short communication (Scientific journals)
Cowden Syndrome: a novel PTEN mutation description and how to recognize a not so rare hereditary cancer syndrome
DELANNOY, Pauline
;
DEBRAY, François-Guillaume
;
BECKERS, Albert
et al.
2014
•
In
Acta Clinica Belgica, 69
(suppl 3), p. 16
Peer Reviewed verified by ORBi
Permalink
https://hdl.handle.net/2268/176510
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Keywords :
cowden syndrome; PTEN; hereditary cancer
Disciplines :
Endocrinology, metabolism & nutrition
Author, co-author :
DELANNOY, Pauline
DEBRAY, François-Guillaume
;
Centre Hospitalier Universitaire de Liège - CHU > Génétique
BECKERS, Albert
;
Centre Hospitalier Universitaire de Liège - CHU > Endocrinologie clinique
VALDES SOCIN, Hernan Gonzalo
;
Centre Hospitalier Universitaire de Liège - CHU > Endocrinologie clinique
Language :
English
Title :
Cowden Syndrome: a novel PTEN mutation description and how to recognize a not so rare hereditary cancer syndrome
Alternative titles :
[en]
Le syndrome de Cowden: une nouvelle mutation décrite et comment reconnaitre un cancer héréditaire pas si rare.
Publication date :
2014
Journal title :
Acta Clinica Belgica
ISSN :
0001-5512
Publisher :
Acta Clinica Belgica, Bruxelles, Belgium
Volume :
69
Issue :
suppl 3
Pages :
S16
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 14 January 2015
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