| 000 | 01791 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250516053417.0 | ||
| 264 | 0 | _c20120327 | |
| 008 | 201203s 0 0 eng d | ||
| 022 | _a1098-1004 | ||
| 024 | 7 |
_a10.1002/humu.21585 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKariminejad, Roxana | |
| 245 | 0 | 0 |
_aHigh frequency of rare copy number variants affecting functionally related genes in patients with structural brain malformations. _h[electronic resource] |
| 260 |
_bHuman mutation _cDec 2011 |
||
| 300 |
_a1427-35 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAgenesis of Corpus Callosum _xdiagnostic imaging |
| 650 | 0 | 4 |
_aBrain _xdiagnostic imaging |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aCohort Studies |
| 650 | 0 | 4 | _aComparative Genomic Hybridization |
| 650 | 0 | 4 |
_aDNA Copy Number Variations _xgenetics |
| 650 | 0 | 4 |
_aEpilepsy _xdiagnostic imaging |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGene Dosage _xgenetics |
| 650 | 0 | 4 | _aGene Frequency |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aIntellectual Disability _xdiagnostic imaging |
| 650 | 0 | 4 | _aMagnetic Resonance Imaging |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aNervous System Malformations _xdiagnostic imaging |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aProteins _xgenetics |
| 650 | 0 | 4 | _aRadiography |
| 650 | 0 | 4 | _aTomography Scanners, X-Ray Computed |
| 700 | 1 | _aLind-Thomsen, Allan | |
| 700 | 1 | _aTümer, Zeynep | |
| 700 | 1 | _aErdogan, Fikret | |
| 700 | 1 | _aRopers, Hans H | |
| 700 | 1 | _aTommerup, Niels | |
| 700 | 1 | _aUllmann, Reinhard | |
| 700 | 1 | _aMøller, Rikke S | |
| 773 | 0 |
_tHuman mutation _gvol. 32 _gno. 12 _gp. 1427-35 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/humu.21585 _zAvailable from publisher's website |
| 999 |
_c21124359 _d21124359 |
||