000			01466 a2200421 4500
005			20250517212853.0
264		0	_c20181012
008			201810s 0 0 eng d
022			_a1435-232X
024	7		_a10.1038/s10038-018-0451-x _2doi
040			_aNLM _beng _cNLM
100	1		_aGillentine, Madelyn A
245	0	0	_aAn estimation of the prevalence of genomic disorders using chromosomal microarray data. _h[electronic resource]
260			_bJournal of human genetics _cJul 2018
300			_a795-801 p. _bdigital
500			_aPublication Type: Journal Article
650	0	4	_aCharcot-Marie-Tooth Disease _xepidemiology
650	0	4	_aChromosome Deletion
650	0	4	_aChromosome Duplication
650	0	4	_aChromosome Mapping
650	0	4	_aDNA Copy Number Variations
650	0	4	_aDiGeorge Syndrome _xepidemiology
650	0	4	_aGenome, Human
650	0	4	_aHumans
650	0	4	_aMicroarray Analysis
650	0	4	_aModels, Genetic
650	0	4	_aMolecular Epidemiology
650	0	4	_aPenetrance
650	0	4	_aPrader-Willi Syndrome _xepidemiology
650	0	4	_aPrevalence
650	0	4	_aSmith-Magenis Syndrome _xepidemiology
650	0	4	_aWilliams Syndrome _xepidemiology
700	1		_aLupo, Philip J
700	1		_aStankiewicz, Pawel
700	1		_aSchaaf, Christian P
773	0		_tJournal of human genetics _gvol. 63 _gno. 7 _gp. 795-801
856	4	0	_uhttps://doi.org/10.1038/s10038-018-0451-x _zAvailable from publisher's website
999			_c28322792 _d28322792