000			01972 a2200589 4500
005			20250515120508.0
264		0	_c20080626
008			200806s 0 0 eng d
022			_a1552-4833
024	7		_a10.1002/ajmg.a.32310 _2doi
040			_aNLM _beng _cNLM
100	1		_aSwinkels, Mariëlle E M
245	0	0	_aClinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype. _h[electronic resource]
260			_bAmerican journal of medical genetics. Part A _cJun 2008
300			_a1430-8 p. _bdigital
500			_aPublication Type: Journal Article
650	0	4	_aAdult
650	0	4	_aChild
650	0	4	_aChild, Preschool
650	0	4	_aChromosome Deletion
650	0	4	_aChromosomes, Human, Pair 9 _xgenetics
650	0	4	_aCraniofacial Abnormalities _xgenetics
650	0	4	_aCytokines _xgenetics
650	0	4	_aDNA Mutational Analysis
650	0	4	_aFemale
650	0	4	_aHumans
650	0	4	_aIn Situ Hybridization, Fluorescence
650	0	4	_aInfant, Newborn
650	0	4	_aIntellectual Disability _xgenetics
650	0	4	_aMale
650	0	4	_aMuscle Hypotonia _xgenetics
650	0	4	_aNetherlands
650	0	4	_aPhenotype
650	0	4	_aSyndrome
700	1		_aSimons, Annet
700	1		_aSmeets, Dominique F
700	1		_aVissers, Lisenka E
700	1		_aVeltman, Joris A
700	1		_aPfundt, Rolph
700	1		_ade Vries, Bert B A
700	1		_aFaas, Brigitte H W
700	1		_aSchrander-Stumpel, Connie T R M
700	1		_aMcCann, Emma
700	1		_aSweeney, Elizabeth
700	1		_aMay, Paul
700	1		_aDraaisma, Jos M
700	1		_aKnoers, Nine V
700	1		_avan Kessel, Ad Geurts
700	1		_avan Ravenswaaij-Arts, Conny M A
773	0		_tAmerican journal of medical genetics. Part A _gvol. 146A _gno. 11 _gp. 1430-8
856	4	0	_uhttps://doi.org/10.1002/ajmg.a.32310 _zAvailable from publisher's website
999			_c17948246 _d17948246