000 01377 a2200433 4500
005 20250516094847.0
264 0 _c20121113
008 201211s 0 0 eng d
022 _a1552-4833
024 7 _a10.1002/ajmg.a.35396
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aDavis, L K
245 0 0 _aRare inherited A2BP1 deletion in a proband with autism and developmental hemiparesis.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cJul 2012
300 _a1654-61 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAutistic Disorder
_xcomplications
650 0 4 _aChild
650 0 4 _aDNA Copy Number Variations
650 0 4 _aGene Deletion
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aParesis
_xcomplications
650 0 4 _aPedigree
650 0 4 _aPhenotype
650 0 4 _aRNA Splicing Factors
650 0 4 _aRNA-Binding Proteins
_xgenetics
700 1 _aMaltman, N
700 1 _aMosconi, M W
700 1 _aMacmillan, C
700 1 _aSchmitt, L
700 1 _aMoore, K
700 1 _aFrancis, S M
700 1 _aJacob, S
700 1 _aSweeney, J A
700 1 _aCook, E H
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 158A
_gno. 7
_gp. 1654-61
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.35396
_zAvailable from publisher's website
999 _c21847697
_d21847697