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	1.	Phenotype comparison confirms ZMYND11 as a critical gene for 10p15.3 microdeletion syndrome. [electronic resource] by Tumiene, Birute Čiuladaitė, Ž Preikšaitienė, E Mameniškienė, R Utkus, A Kučinskas, V Producer: 20180201 In: Journal of applied genetics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Two new de novo interstitial duplications covering 2p14-p22.1: clinical and molecular analysis. [electronic resource] by Kasnauskiene, J Cimbalistiene, L Utkus, A Ciuladaite, Z Preiksaitiene, E Pečiulytė, A Kučinskas, V Producer: 20130204 In: Cytogenetic and genome research vol. 139 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel de novo 1.8 Mb microdeletion of 17q21.33 associated with intellectual disability and dysmorphic features. [electronic resource] by Preiksaitiene, E Männik, K Dirse, V Utkus, A Ciuladaite, Z Kasnauskiene, J Kurg, A Kučinskas, V Producer: 20130218 In: European journal of medical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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