Publikuoti straipsniai:

1. Preiksaitiene E, Molyte A, Kasnauskiene J, Ciuladaite Z, Utkus A, Patsalis PC, Kučinskas V. Considering specific clinical features as evidence of pathogenic copy number variants. J Appl Genet. 2014 May; 55(2):189-96. doi: 10.1007/s13353-014-0197-x. Epub 2014 Feb 18.
2. Ciuladaite Z, Preiksaitiene E, Utkus A, Kučinskas V. Relatives with Opposite Chromosome Constitutions, rec(10)dup(10p)inv(10)(p15.1q26.12) and rec(10)dup(10q)inv(10)(p15.1q26.12), due to a Familial Pericentric Inversion. Cytogenet Genome Res. 2014; 144(2):109-13. doi: 10.1159/000368863. Epub 2014 Nov 15.
3. Preiksaitiene E, Krasovskaja N, Utkus A, Kasnauskiene J, Meskienė R, Paulauskiene I, Valeviciene NR, Kučinskas V. R368X mutation in MID1 among recurrent mutations in patients with X-linked Opitz G/BBB syndrome. Clin Dysmorphol. 2014 Oct 9.