| 000 | 01759 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250515070229.0 | ||
| 264 | 0 | _c20080422 | |
| 008 | 200804s 0 0 eng d | ||
| 022 | _a1601-183X | ||
| 024 | 7 |
_a10.1111/j.1601-183X.2007.00326.x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aZinkstok, J | |
| 245 | 0 | 0 |
_aGenetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia. _h[electronic resource] |
| 260 |
_bGenes, brain, and behavior _cFeb 2008 |
||
| 300 |
_a61-9 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAlleles |
| 650 | 0 | 4 |
_aCatechol O-Methyltransferase _xgenetics |
| 650 | 0 | 4 |
_aCerebral Cortex _xpathology |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 22 |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 |
_aDominance, Cerebral _xgenetics |
| 650 | 0 | 4 | _aEpistasis, Genetic |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGene Frequency _xgenetics |
| 650 | 0 | 4 | _aGenetic Carrier Screening |
| 650 | 0 | 4 |
_aGenetic Predisposition to Disease _xgenetics |
| 650 | 0 | 4 |
_aGenetic Variation _xgenetics |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aImage Processing, Computer-Assisted |
| 650 | 0 | 4 | _aMagnetic Resonance Imaging |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aPolymorphism, Single Nucleotide _xgenetics |
| 650 | 0 | 4 |
_aProline Oxidase _xgenetics |
| 650 | 0 | 4 |
_aPsychotic Disorders _xdiagnosis |
| 650 | 0 | 4 |
_aSchizophrenia _xdiagnosis |
| 700 | 1 | _aSchmitz, N | |
| 700 | 1 | _avan Amelsvoort, T | |
| 700 | 1 | _aMoeton, M | |
| 700 | 1 | _aBaas, F | |
| 700 | 1 | _aLinszen, D | |
| 773 | 0 |
_tGenes, brain, and behavior _gvol. 7 _gno. 1 _gp. 61-9 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1601-183X.2007.00326.x _zAvailable from publisher's website |
| 999 |
_c17048842 _d17048842 |
||