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.
2014In Acta Clinica Belgica, 69 (suppl 3), p. 16
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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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