| 000 | 01806 a2200565 4500 | ||
|---|---|---|---|
| 005 | 20250516064222.0 | ||
| 264 | 0 | _c20130107 | |
| 008 | 201301s 0 0 eng d | ||
| 022 | _a1399-0004 | ||
| 024 | 7 |
_a10.1111/j.1399-0004.2011.01810.x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aDe Filippis, R | |
| 245 | 0 | 0 |
_aExpanding the phenotype associated with FOXG1 mutations and in vivo FoxG1 chromatin-binding dynamics. _h[electronic resource] |
| 260 |
_bClinical genetics _cOct 2012 |
||
| 300 |
_a395-403 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aBlotting, Western |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 |
_aChromatin _xmetabolism |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 15 _xgenetics |
| 650 | 0 | 4 |
_aDNA Methylation _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aFluorescence Recovery After Photobleaching |
| 650 | 0 | 4 |
_aForkhead Transcription Factors _xgenetics |
| 650 | 0 | 4 |
_aGenetic Diseases, Inborn _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aKaryotyping |
| 650 | 0 | 4 | _aMicroscopy, Fluorescence |
| 650 | 0 | 4 |
_aNerve Tissue Proteins _xgenetics |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aPoint Mutation _xgenetics |
| 650 | 0 | 4 | _aSyndrome |
| 700 | 1 | _aPancrazi, L | |
| 700 | 1 | _aBjørgo, K | |
| 700 | 1 | _aRosseto, A | |
| 700 | 1 | _aKleefstra, T | |
| 700 | 1 | _aGrillo, E | |
| 700 | 1 | _aPanighini, A | |
| 700 | 1 | _aCardarelli, F | |
| 700 | 1 | _aMeloni, I | |
| 700 | 1 | _aAriani, F | |
| 700 | 1 | _aMencarelli, M A | |
| 700 | 1 | _aHayek, J | |
| 700 | 1 | _aRenieri, A | |
| 700 | 1 | _aCosta, M | |
| 700 | 1 | _aMari, F | |
| 773 | 0 |
_tClinical genetics _gvol. 82 _gno. 4 _gp. 395-403 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1399-0004.2011.01810.x _zAvailable from publisher's website |
| 999 |
_c21319534 _d21319534 |
||