Delannoy, Pauline <br/><br/>
How to recognize Cowden syndrome: A novel PTEN mutation description.  [electronic resource] 

 -  Annales d'endocrinologie  Jul 2017 
 - 188-190 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>2213-3941 
<br/><br/><label>Standard No.: </label>10.1016/j.ando.2017.01.001  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Female<br/>Hamartoma Syndrome, Multiple--diagnosis<br/>Humans<br/>Mutation<br/>PTEN Phosphohydrolase--genetics<br/>Young Adult