000 01528 a2200445 4500
005 20250516092504.0
264 0 _c20120924
008 201209s 0 0 eng d
022 _a1552-4833
024 7 _a10.1002/ajmg.a.35365
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aOegema, Renske
245 0 0 _aAsymmetric polymicrogyria and periventricular nodular heterotopia due to mutation in ARX.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cJun 2012
300 _a1472-6 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aFacies
650 0 4 _aHeterozygote
650 0 4 _aHomeodomain Proteins
_xgenetics
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aKaryotype
650 0 4 _aMale
650 0 4 _aMalformations of Cortical Development
_xdiagnosis
650 0 4 _aMutagenesis, Insertional
650 0 4 _aMutation
650 0 4 _aNeuroimaging
650 0 4 _aPeriventricular Nodular Heterotopia
_xdiagnosis
650 0 4 _aTranscription Factors
_xgenetics
700 1 _aMaat-Kievit, Anneke
700 1 _aLequin, Maarten H
700 1 _aSchot, Rachel
700 1 _aNanninga-van den Neste, Veerle M H
700 1 _aDoornbos, Marianne E
700 1 _ade Wit, Marie C Y
700 1 _aHalley, Dicky J
700 1 _aMancini, Grazia M S
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 158A
_gno. 6
_gp. 1472-6
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.35365
_zAvailable from publisher's website
999 _c21781010
_d21781010