000			02253 a2200673 4500
005			20250518055208.0
264		0	_c20200615
008			202006s 0 0 eng d
022			_a1468-6244
024	7		_a10.1136/jmedgenet-2018-105879 _2doi
040			_aNLM _beng _cNLM
100	1		_aJønch, Aia Elise
245	0	0	_aEstimating the effect size of the 15Q11.2 BP1-BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice. _h[electronic resource]
260			_bJournal of medical genetics _c10 2019
300			_a701-710 p. _bdigital
500			_aPublication Type: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't
650	0	4	_aAutistic Disorder _xgenetics
650	0	4	_aCase-Control Studies
650	0	4	_aCohort Studies
650	0	4	_aDNA Copy Number Variations
650	0	4	_aEpilepsy _xgenetics
650	0	4	_aFemale
650	0	4	_aHeart Diseases _xcongenital
650	0	4	_aHumans
650	0	4	_aIntellectual Disability _xgenetics
650	0	4	_aLoss of Function Mutation
650	0	4	_aMale
650	0	4	_aNeurodevelopmental Disorders _xgenetics
650	0	4	_aSequence Deletion
700	1		_aDouard, Elise
700	1		_aMoreau, Clara
700	1		_aVan Dijck, Anke
700	1		_aPasseggeri, Marzia
700	1		_aKooy, Frank
700	1		_aPuechberty, Jacques
700	1		_aCampbell, Carolyn
700	1		_aSanlaville, Damien
700	1		_aLefroy, Henrietta
700	1		_aRichetin, Sonia
700	1		_aPain, Aurelie
700	1		_aGeneviève, David
700	1		_aKini, Usha
700	1		_aLe Caignec, Cédric
700	1		_aLespinasse, James
700	1		_aSkytte, Anne-Bine
700	1		_aIsidor, Bertrand
700	1		_aZweier, Christiane
700	1		_aCaberg, Jean-Hubert
700	1		_aDelrue, Marie-Ange
700	1		_aMøller, Rikke Steensbjerre
700	1		_aBojesen, Anders
700	1		_aHjalgrim, Helle
700	1		_aBrasch-Andersen, Charlotte
700	1		_aLemyre, Emmanuelle
700	1		_aOusager, Lilian Bomme
700	1		_aJacquemont, Sébastien
773	0		_tJournal of medical genetics _gvol. 56 _gno. 10 _gp. 701-710
856	4	0	_uhttps://doi.org/10.1136/jmedgenet-2018-105879 _zAvailable from publisher's website
999			_c30043671 _d30043671