| 000 | 01067 a2200313 4500 | ||
|---|---|---|---|
| 005 | 20250517142304.0 | ||
| 264 | 0 | _c20190103 | |
| 008 | 201901s 0 0 eng d | ||
| 022 | _a2213-3941 | ||
| 024 | 7 |
_a10.1016/j.ando.2017.01.001 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aDelannoy, Pauline | |
| 245 | 0 | 0 |
_aHow to recognize Cowden syndrome: A novel PTEN mutation description. _h[electronic resource] |
| 260 |
_bAnnales d'endocrinologie _cJul 2017 |
||
| 300 |
_a188-190 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Letter | ||
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aHamartoma Syndrome, Multiple _xdiagnosis |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aPTEN Phosphohydrolase _xgenetics |
| 650 | 0 | 4 | _aYoung Adult |
| 700 | 1 | _aDebray, François Guillaume | |
| 700 | 1 | _aVerloes, Alain | |
| 700 | 1 | _aBeckers, Albert | |
| 700 | 1 | _aValdes-Socin, Hernan | |
| 773 | 0 |
_tAnnales d'endocrinologie _gvol. 78 _gno. 3 _gp. 188-190 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ando.2017.01.001 _zAvailable from publisher's website |
| 999 |
_c26938021 _d26938021 |
||