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; VALDES SOCIN, Hernan Gonzalo

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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

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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 :

Issue :

suppl 3

Pages :

S16

Peer reviewed :

Peer Reviewed verified by ORBi

Available on ORBi :

since 14 January 2015

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