000			01530 a2200433 4500
005			20250515015553.0
264		0	_c20061120
008			200611s 0 0 eng d
022			_a1769-7212
024	7		_a10.1016/j.ejmg.2006.01.005 _2doi
040			_aNLM _beng _cNLM
100	1		_aFeenstra, I
245	0	0	_aCryptic duplication of the distal segment of 22q due to a translocation (21;22): three case reports and a review of the literature. _h[electronic resource]
260			_bEuropean journal of medical genetics _c
300			_a384-95 p. _bdigital
500			_aPublication Type: Case Reports; Journal Article; Review
650	0	4	_aAbnormalities, Multiple _xgenetics
650	0	4	_aAdult
650	0	4	_aAneuploidy
650	0	4	_aChild, Preschool
650	0	4	_aChromosomes, Human, Pair 21 _xgenetics
650	0	4	_aChromosomes, Human, Pair 22 _xgenetics
650	0	4	_aDevelopmental Disabilities _xgenetics
650	0	4	_aFace _xabnormalities
650	0	4	_aFemale
650	0	4	_aHumans
650	0	4	_aIn Situ Hybridization, Fluorescence
650	0	4	_aIntellectual Disability _xgenetics
650	0	4	_aMale
650	0	4	_aTranslocation, Genetic
700	1		_aKoolen, D A
700	1		_aVan der Pas, J
700	1		_aHamel, B C J
700	1		_aMieloo, H
700	1		_aSmeets, D F C M
700	1		_aVan Ravenswaaij, C M A
773	0		_tEuropean journal of medical genetics _gvol. 49 _gno. 5 _gp. 384-95
856	4	0	_uhttps://doi.org/10.1016/j.ejmg.2006.01.005 _zAvailable from publisher's website
999			_c16113877 _d16113877