000			02052 a2200613 4500
005			20250517000450.0
264		0	_c20150528
008			201505s 0 0 eng d
022			_a1468-2044
024	7		_a10.1136/archdischild-2014-306810 _2doi
040			_aNLM _beng _cNLM
100	1		_aLaffargue, Fanny
245	0	0	_aTowards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome. _h[electronic resource]
260			_bArchives of disease in childhood _cMar 2015
300			_a259-64 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650	0	4	_aAdolescent
650	0	4	_aCentral Nervous System Diseases _xcomplications
650	0	4	_aChild
650	0	4	_aChild, Preschool
650	0	4	_aChromosome Deletion
650	0	4	_aChromosomes, Human, Pair 17 _xgenetics
650	0	4	_aDental Enamel _xabnormalities
650	0	4	_aDiabetes Mellitus, Type 2 _xcomplications
650	0	4	_aFemale
650	0	4	_aFrance
650	0	4	_aHepatocyte Nuclear Factor 1-beta _xgenetics
650	0	4	_aHumans
650	0	4	_aIn Situ Hybridization, Fluorescence
650	0	4	_aInfant
650	0	4	_aKidney Diseases, Cystic _xcomplications
650	0	4	_aMale
650	0	4	_aMental Disorders _xgenetics
650	0	4	_aPhenotype
650	0	4	_aProspective Studies
700	1		_aBourthoumieu, Sylvie
700	1		_aLlanas, Brigitte
700	1		_aBaudouin, Véronique
700	1		_aLahoche, Annie
700	1		_aMorin, Denis
700	1		_aBessenay, Lucie
700	1		_aDe Parscau, Loïc
700	1		_aCloarec, Sylvie
700	1		_aDelrue, Marie-Ange
700	1		_aTaupiac, Emmanuelle
700	1		_aDizier, Emilie
700	1		_aLaroche, Cécile
700	1		_aBahans, Claire
700	1		_aYardin, Catherine
700	1		_aLacombe, Didier
700	1		_aGuigonis, Vincent
773	0		_tArchives of disease in childhood _gvol. 100 _gno. 3 _gp. 259-64
856	4	0	_uhttps://doi.org/10.1136/archdischild-2014-306810 _zAvailable from publisher's website
999			_c24287320 _d24287320