| 000 | 01687 a2200553 4500 | ||
|---|---|---|---|
| 005 | 20250515115027.0 | ||
| 264 | 0 | _c20080522 | |
| 008 | 200805s 0 0 eng d | ||
| 022 | _a1552-4833 | ||
| 024 | 7 |
_a10.1002/ajmg.a.32264 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMerello, Elisa | |
| 245 | 0 | 0 |
_aNo major role for the EMX2 gene in schizencephaly. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics. Part A _cMay 2008 |
||
| 300 |
_a1142-50 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAnimals |
| 650 | 0 | 4 |
_aBrain _xabnormalities |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aHomeodomain Proteins _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMalformations of Cortical Development _xetiology |
| 650 | 0 | 4 | _aMice |
| 650 | 0 | 4 | _aMice, Knockout |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 |
_aTranscription Factors _xdeficiency |
| 700 | 1 | _aSwanson, Eric | |
| 700 | 1 | _aDe Marco, Patrizia | |
| 700 | 1 | _aAkhter, Murtaza | |
| 700 | 1 | _aStriano, Pasquale | |
| 700 | 1 | _aRossi, Andrea | |
| 700 | 1 | _aCama, Armando | |
| 700 | 1 | _aLeventer, Richard J | |
| 700 | 1 | _aGuerrini, Renzo | |
| 700 | 1 | _aCapra, Valeria | |
| 700 | 1 | _aDobyns, William B | |
| 773 | 0 |
_tAmerican journal of medical genetics. Part A _gvol. 146A _gno. 9 _gp. 1142-50 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.a.32264 _zAvailable from publisher's website |
| 999 |
_c17907398 _d17907398 |
||