| 000 | 01464 a2200409 4500 | ||
|---|---|---|---|
| 005 | 20250515230028.0 | ||
| 264 | 0 | _c20110111 | |
| 008 | 201101s 0 0 eng d | ||
| 022 | _a1878-0849 | ||
| 024 | 7 |
_a10.1016/j.ejmg.2010.05.003 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aGerkes, Erica H | |
| 245 | 0 | 0 |
_aBilateral polymicrogyria as the indicative feature in a child with a 22q11.2 deletion. _h[electronic resource] |
| 260 |
_bEuropean journal of medical genetics _c |
||
| 300 |
_a344-6 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aCerebral Cortex _xabnormalities |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 22 |
| 650 | 0 | 4 |
_aDevelopmental Disabilities _xgenetics |
| 650 | 0 | 4 |
_aDiGeorge Syndrome _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aMagnetic Resonance Imaging |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMalformations of Cortical Development _xgenetics |
| 650 | 0 | 4 |
_aMicrocephaly _xgenetics |
| 700 | 1 | _aHordijk, Roel | |
| 700 | 1 | _aDijkhuizen, Trijnie | |
| 700 | 1 | _aSival, Deborah A | |
| 700 | 1 | _aMeiners, Linda C | |
| 700 | 1 | _aSikkema-Raddatz, Birgit | |
| 700 | 1 | _avan Ravenswaaij-Arts, Conny M A | |
| 773 | 0 |
_tEuropean journal of medical genetics _gvol. 53 _gno. 5 _gp. 344-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ejmg.2010.05.003 _zAvailable from publisher's website |
| 999 |
_c19903112 _d19903112 |
||