| 000 | 01843 a2200541 4500 | ||
|---|---|---|---|
| 005 | 20250516163006.0 | ||
| 264 | 0 | _c20140513 | |
| 008 | 201405s 0 0 eng d | ||
| 022 | _a1879-1379 | ||
| 024 | 7 |
_a10.1016/j.jpsychires.2013.07.004 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aZarchi, Omer | |
| 245 | 0 | 0 |
_aSchizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes. _h[electronic resource] |
| 260 |
_bJournal of psychiatric research _cNov 2013 |
||
| 300 |
_a1623-9 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_a22q11 Deletion Syndrome _xgenetics |
| 650 | 0 | 4 | _aAcoustic Stimulation |
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aCatechol O-Methyltransferase _xgenetics |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 |
_aContingent Negative Variation _xgenetics |
| 650 | 0 | 4 | _aEndophenotypes |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Association Studies |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aPolymorphism, Single Nucleotide _xgenetics |
| 650 | 0 | 4 |
_aProline Oxidase _xgenetics |
| 650 | 0 | 4 |
_aSchizophrenia _xphysiopathology |
| 650 | 0 | 4 |
_aSensory Gating _xgenetics |
| 650 | 0 | 4 | _aYoung Adult |
| 700 | 1 | _aCarmel, Miri | |
| 700 | 1 | _aAvni, Chen | |
| 700 | 1 | _aAttias, Josef | |
| 700 | 1 | _aFrisch, Amos | |
| 700 | 1 | _aMichaelovsky, Elena | |
| 700 | 1 | _aPatya, Miriam | |
| 700 | 1 | _aGreen, Tamar | |
| 700 | 1 | _aWeinberger, Ronnie | |
| 700 | 1 | _aWeizman, Abraham | |
| 700 | 1 | _aGothelf, Doron | |
| 773 | 0 |
_tJournal of psychiatric research _gvol. 47 _gno. 11 _gp. 1623-9 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.jpsychires.2013.07.004 _zAvailable from publisher's website |
| 999 |
_c22971260 _d22971260 |
||