1. A prenatally diagnosed case of Meckel–Gruber syndrome with novel compound heterozygous pathogenic variants in the TXNDC15 gene. Issue 5 (9th March 2019) Authors: Ridnõi, Konstantin; Šois, Marek; Vaidla, Eve; Pajusalu, Sander; Kelder, Larissa; Reimand, Tiia; Õunap, Katrin Journal: Molecular genetics & genomic medicine Issue: Volume 7:Issue 5(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Chromosomal microarray analysis as a first‐tier clinical diagnostic test: Estonian experience. Issue 2 (9th January 2014) Authors: Žilina, Olga; Teek, Rita; Tammur, Pille; Kuuse, Kati; Yakoreva, Maria; Vaidla, Eve; Mölter‐Väär, Triin; Reimand, Tiia; Kurg, Ants; Õunap, Katrin Journal: Molecular genetics & genomic medicine Issue: Volume 2:Issue 2(2014:Mar.) Page Start: 166 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗