000			02231 a2200709 4500
005			20250516050539.0
264		0	_c20120531
008			201205s 0 0 eng d
022			_a1098-1004
024	7		_a10.1002/humu.21568 _2doi
040			_aNLM _beng _cNLM
100	1		_aGuo, Tingwei
245	0	0	_aGenotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. _h[electronic resource]
260			_bHuman mutation _cNov 2011
300			_a1278-89 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, N.I.H., Extramural
650	0	4	_a22q11 Deletion Syndrome _xgenetics
650	0	4	_aCardiovascular Abnormalities _xgenetics
650	0	4	_aChromosomes, Human, Pair 22 _xgenetics
650	0	4	_aDiGeorge Syndrome _xgenetics
650	0	4	_aGenetic Variation
650	0	4	_aGenotype
650	0	4	_aHaplotypes
650	0	4	_aHumans
650	0	4	_aPhenotype
650	0	4	_aPolymorphism, Single Nucleotide
650	0	4	_aT-Box Domain Proteins _xgenetics
700	1		_aMcDonald-McGinn, Donna
700	1		_aBlonska, Anna
700	1		_aShanske, Alan
700	1		_aBassett, Anne S
700	1		_aChow, Eva
700	1		_aBowser, Mark
700	1		_aSheridan, Molly
700	1		_aBeemer, Frits
700	1		_aDevriendt, Koen
700	1		_aSwillen, Ann
700	1		_aBreckpot, Jeroen
700	1		_aDigilio, Maria C
700	1		_aMarino, Bruno
700	1		_aDallapiccola, Bruno
700	1		_aCarpenter, Courtney
700	1		_aZheng, Xin
700	1		_aJohnson, Jacob
700	1		_aChung, Jonathan
700	1		_aHiggins, Anne Marie
700	1		_aPhilip, Nicole
700	1		_aSimon, Tony J
700	1		_aColeman, Karlene
700	1		_aHeine-Suner, Damian
700	1		_aRosell, Jordi
700	1		_aKates, Wendy
700	1		_aDevoto, Marcella
700	1		_aGoldmuntz, Elizabeth
700	1		_aZackai, Elaine
700	1		_aWang, Tao
700	1		_aShprintzen, Robert
700	1		_aEmanuel, Beverly
700	1		_aMorrow, Bernice
773	0		_tHuman mutation _gvol. 32 _gno. 11 _gp. 1278-89
856	4	0	_uhttps://doi.org/10.1002/humu.21568 _zAvailable from publisher's website
999			_c21042692 _d21042692