000 01840 a2200421 4500
005 20250515230004.0
264 0 _c20110113
008 201101s 0 0 eng d
022 _a1552-485X
024 7 _a10.1002/ajmg.b.31107
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aCocchella, Alessandro
245 0 0 _aThe refinement of the critical region for the 2q31.2q32.3 deletion syndrome indicates candidate genes for mental retardation and speech impairment.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
_cOct 2010
300 _a1342-6 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aBasic Helix-Loop-Helix Transcription Factors
_xgenetics
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 2
650 0 4 _aCyclic Nucleotide Phosphodiesterases, Type 1
_xgenetics
650 0 4 _aFemale
650 0 4 _aGenetic Association Studies
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aKruppel-Like Transcription Factors
_xgenetics
650 0 4 _aSpeech Disorders
_xgenetics
700 1 _aMalacarne, Michela
700 1 _aForzano, Francesca
700 1 _aMarciano, Carmela
700 1 _aPierluigi, Mauro
700 1 _aPerroni, Lucia
700 1 _aFaravelli, Francesca
700 1 _aDi Maria, Emilio
773 0 _tAmerican journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
_gvol. 153B
_gno. 7
_gp. 1342-6
856 4 0 _uhttps://doi.org/10.1002/ajmg.b.31107
_zAvailable from publisher's website
999 _c19901859
_d19901859