TY  - GEN
AU  - Delannoy,Pauline
AU  - Debray,François Guillaume
AU  - Verloes,Alain
AU  - Beckers,Albert
AU  - Valdes-Socin,Hernan
TI  - How to recognize Cowden syndrome: A novel PTEN mutation description
SN  - 2213-3941
PY  - 2019///0103
KW  - Female
KW  - Hamartoma Syndrome, Multiple
KW  - diagnosis
KW  - Humans
KW  - Mutation
KW  - PTEN Phosphohydrolase
KW  - genetics
KW  - Young Adult
N1  - Publication Type: Case Reports; Letter
UR  - https://doi.org/10.1016/j.ando.2017.01.001
ER  -