An 8.4‐Mb 3q26.33‐3q28 microdeletion in a patient with blepharophimosis–intellectual disability syndrome and a review of the literature

por Õunap, Katrin, Pajusalu, Sander, Zilina, Olga, Reimand, Tiia, Žordania, Riina
Publicado 2016

Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome

por Žilina, Olga, Koltšina, Marina, Raid, Raivo, Kurg, Ants, Tõnisson, Neeme, Salumets, Andres
Publicado 2015

Chromosomal microarray analysis as a first-tier clinical diagnostic test: Estonian experience

por Žilina, Olga, Teek, Rita, Tammur, Pille, Kuuse, Kati, Yakoreva, Maria, Vaidla, Eve, Mölter-Väär, Triin, Reimand, Tiia, Kurg, Ants, Õunap, Katrin
Publicado 2014

NIPTmer: rapid k-mer-based software package for detection of fetal aneuploidies

por Sauk, Martin, Žilina, Olga, Kurg, Ants, Ustav, Eva-Liina, Peters, Maire, Paluoja, Priit, Roost, Anne Mari, Teder, Hindrek, Palta, Priit, Brison, Nathalie, Vermeesch, Joris R., Krjutškov, Kaarel, Salumets, Andres, Kaplinski, Lauris
Publicado 2018