000 | 01779 a2200517 4500 | ||
---|---|---|---|
005 | 20250515043630.0 | ||
264 | 0 | _c20070222 | |
008 | 200702s 0 0 eng d | ||
022 | _a1617-4615 | ||
024 | 7 |
_a10.1007/s00438-006-0173-1 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aPetek, Erwin | |
245 | 0 | 0 |
_aMolecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome. _h[electronic resource] |
260 |
_bMolecular genetics and genomics : MGG _cJan 2007 |
||
300 |
_a71-81 p. _bdigital |
||
500 | _aPublication Type: Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 |
_aAutistic Disorder _xgenetics |
650 | 0 | 4 | _aCell Line |
650 | 0 | 4 |
_aChromosomes, Human, Pair 7 _xgenetics |
650 | 0 | 4 | _aDNA Mutational Analysis |
650 | 0 | 4 |
_aEndopeptidases _xgenetics |
650 | 0 | 4 | _aGene Duplication |
650 | 0 | 4 |
_aGene Expression Regulation _xgenetics |
650 | 0 | 4 | _aGenetic Predisposition to Disease |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aHybridomas |
650 | 0 | 4 | _aMutation |
650 | 0 | 4 | _aQuantitative Trait Loci |
650 | 0 | 4 |
_aTourette Syndrome _xgenetics |
700 | 1 | _aSchwarzbraun, Thomas | |
700 | 1 | _aNoor, Abdul | |
700 | 1 | _aPatel, Megha | |
700 | 1 | _aNakabayashi, Kazuhiko | |
700 | 1 | _aChoufani, Sanaa | |
700 | 1 | _aWindpassinger, Christian | |
700 | 1 | _aStamenkovic, Mara | |
700 | 1 | _aRobertson, Mary M | |
700 | 1 | _aAschauer, Harald N | |
700 | 1 | _aGurling, Hugh M D | |
700 | 1 | _aKroisel, Peter M | |
700 | 1 | _aWagner, Klaus | |
700 | 1 | _aScherer, Stephen W | |
700 | 1 | _aVincent, John B | |
773 | 0 |
_tMolecular genetics and genomics : MGG _gvol. 277 _gno. 1 _gp. 71-81 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1007/s00438-006-0173-1 _zAvailable from publisher's website |
999 |
_c16619736 _d16619736 |