000 01320 a2200385 4500
005 20250516202027.0
264 0 _c20140605
008 201406s 0 0 eng d
022 _a1879-0038
024 7 _a10.1016/j.gene.2014.02.058
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSilva, Isabela M W
245 0 0 _aA 1.5Mb terminal deletion of 12p associated with autism spectrum disorder.
_h[electronic resource]
260 _bGene
_cMay 2014
300 _a83-6 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdaptor Proteins, Signal Transducing
_xgenetics
650 0 4 _aChild
650 0 4 _aChild Development Disorders, Pervasive
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 12
_xgenetics
650 0 4 _aDevelopmental Disabilities
_xgenetics
650 0 4 _aGenetic Association Studies
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aHumans
650 0 4 _aKaryotype
650 0 4 _aMale
650 0 4 _aNerve Tissue Proteins
_xgenetics
700 1 _aRosenfeld, Jill
700 1 _aAntoniuk, Sergio A
700 1 _aRaskin, Salmo
700 1 _aSotomaior, Vanessa S
773 0 _tGene
_gvol. 542
_gno. 1
_gp. 83-6
856 4 0 _uhttps://doi.org/10.1016/j.gene.2014.02.058
_zAvailable from publisher's website
999 _c23625807
_d23625807