Publications
Published data:
- 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.
- 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.
- 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.