000			01975 a2200553 4500
005			20250514073503.0
264		0	_c20040324
008			200403s 0 0 eng d
022			_a1098-3600
024	7		_a10.1097/01.GIM.0000076975.10224.67 _2doi
040			_aNLM _beng _cNLM
100	1		_aHirota, Hamao
245	0	0	_aWilliams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23. _h[electronic resource]
260			_bGenetics in medicine : official journal of the American College of Medical Genetics _c
300			_a311-21 p. _bdigital
500			_aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650	0	4	_aAdolescent
650	0	4	_aAdult
650	0	4	_aChild
650	0	4	_aChromosome Mapping
650	0	4	_aChromosomes, Human, Pair 7
650	0	4	_aCohort Studies
650	0	4	_aCosmids
650	0	4	_aFemale
650	0	4	_aGene Deletion
650	0	4	_aGene Dosage
650	0	4	_aHumans
650	0	4	_aIn Situ Hybridization, Fluorescence
650	0	4	_aIntelligence Tests
650	0	4	_aModels, Genetic
650	0	4	_aMuscle Proteins _xgenetics
650	0	4	_aNuclear Proteins _xgenetics
650	0	4	_aPhenotype
650	0	4	_aPhysical Chromosome Mapping
650	0	4	_aTrans-Activators _xgenetics
650	0	4	_aTranscription Factors, TFII _xgenetics
650	0	4	_aWilliams Syndrome _xdiagnosis
700	1		_aMatsuoka, Rumiko
700	1		_aChen, Xiao-Ning
700	1		_aSalandanan, Lora S
700	1		_aLincoln, Alan
700	1		_aRose, Fredric E
700	1		_aSunahara, Mariko
700	1		_aOsawa, Makiko
700	1		_aBellugi, Ursula
700	1		_aKorenberg, Julie R
773	0		_tGenetics in medicine : official journal of the American College of Medical Genetics _gvol. 5 _gno. 4 _gp. 311-21
856	4	0	_uhttps://doi.org/10.1097/01.GIM.0000076975.10224.67 _zAvailable from publisher's website
999			_c12643624 _d12643624