Voula Velissariou
31 Neas Engomis Street
Egkomi, 2409, Cyprus
Egkomi, 2409, Cyprus
Last Updated: 09/26/2026
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Found 16 publications
Low-Level Trisomy 14 Mosaicism: A Carrier of an Isochromosome 14 and a Supernumerary Marker Chromosome 14.
Journal: Cytogenetic and genome research
Published: June 09, 2020
Novel pericentric inversion inv(9)(p23q22.3) in unrelated individuals with fertility problems in the Southeast European population.
Journal: Journal of human genetics
Published: November 28, 2019
Targeted capture enrichment followed by NGS: development and validation of a single comprehensive NIPT for chromosomal aneuploidies, microdeletion syndromes and monogenic diseases.
Journal: Molecular cytogenetics
Published: June 10, 2019
Unbalanced X;9 translocation in an infertile male with de novo duplication Xp22.31p22.33.
Journal: Journal of assisted reproduction and genetics
Published: October 23, 2018
Cell-Free DNA Analysis of Targeted Genomic Regions in Maternal Plasma for Non-Invasive Prenatal Testing of Trisomy 21, Trisomy 18, Trisomy 13, and Fetal Sex.
Journal: Clinical chemistry
Published: November 26, 2015
A prenatally ascertained de novo terminal deletion of chromosomal bands 1q43q44 associated with multiple congenital abnormalities in a female fetus.
Journal: Case reports in genetics
Published: October 21, 2014
Mandibulofacial dysostosis (Treacher-Collins syndrome) in the fetus: novel association with Pectus carinatum in a molecularly confirmed case and review of the fetal phenotype.
Journal: Birth defects research. Part A, Clinical and molecular teratology
Published: July 16, 2013
Comment on "technical concerns on the clinical validation of the NIFTY test".
Journal: Prenatal diagnosis
Published: April 10, 2013
Clinical and molecular description of the prenatal diagnosis of a fetus with a maternally inherited microduplication 22q11.2 of 2.5 Mb.
Journal: Gene
Published: January 03, 2013
Last Updated: 09/26/2026