000			02327 a2200745 4500
005			20250515191044.0
264		0	_c20100224
008			201002s 0 0 eng d
022			_a1476-5438
024	7		_a10.1038/ejhg.2009.152 _2doi
040			_aNLM _beng _cNLM
100	1		_avan Bon, Bregje W M
245	0	0	_aThe 2q23.1 microdeletion syndrome: clinical and behavioural phenotype. _h[electronic resource]
260			_bEuropean journal of human genetics : EJHG _cFeb 2010
300			_a163-70 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650	0	4	_aAngelman Syndrome _xgenetics
650	0	4	_aCesarean Section
650	0	4	_aChild
650	0	4	_aChromosome Mapping
650	0	4	_aChromosomes, Human, Pair 2 _xgenetics
650	0	4	_aFemale
650	0	4	_aHumans
650	0	4	_aInfant, Newborn
650	0	4	_aIntellectual Disability _xgenetics
650	0	4	_aIntensive Care Units, Neonatal
650	0	4	_aLearning Disabilities _xgenetics
650	0	4	_aMale
650	0	4	_aPhenotype
650	0	4	_aRett Syndrome _xgenetics
650	0	4	_aSequence Deletion
700	1		_aKoolen, David A
700	1		_aBrueton, Louise
700	1		_aMcMullan, Dominic
700	1		_aLichtenbelt, Klaske D
700	1		_aAdès, Lesley C
700	1		_aPeters, Gregory
700	1		_aGibson, Kate
700	1		_aMoloney, Susan
700	1		_aNovara, Francesca
700	1		_aPramparo, Tiziano
700	1		_aDalla Bernardina, Bernardo
700	1		_aZoccante, Leonardo
700	1		_aBalottin, Umberto
700	1		_aPiazza, Fausta
700	1		_aPecile, Vanna
700	1		_aGasparini, Paolo
700	1		_aGuerci, Veronica
700	1		_aKets, Marleen
700	1		_aPfundt, Rolph
700	1		_ade Brouwer, Arjan P
700	1		_aVeltman, Joris A
700	1		_ade Leeuw, Nicole
700	1		_aWilson, Meredith
700	1		_aAntony, Jayne
700	1		_aReitano, Santina
700	1		_aLuciano, Daniela
700	1		_aFichera, Marco
700	1		_aRomano, Corrado
700	1		_aBrunner, Han G
700	1		_aZuffardi, Orsetta
700	1		_ade Vries, Bert B A
773	0		_tEuropean journal of human genetics : EJHG _gvol. 18 _gno. 2 _gp. 163-70
856	4	0	_uhttps://doi.org/10.1038/ejhg.2009.152 _zAvailable from publisher's website
999			_c19204402 _d19204402