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Olga Žilina

Showing results (1-10 of 10) with videos related to

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European Journal of Medical Genetics|February 2, 2013
Patient with dup(5)(q35.2-q35.3) reciprocal to the common Sotos syndrome deletion and review of the literatureOlga Žilina, Tiia Reimand, Pille Tammur, et al.
BMC Genomics|September 18, 2015
Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genomeOlga Žilina, Marina Koltšina, Raivo Raid, et al.
Molecular Syndromology|September 6, 2018
A New Case of a Rare Combination of Temple Syndrome and Mosaic Trisomy 14 and a Literature ReviewMaria Yakoreva, Tiina Kahre, Sander Pajusalu, et al.
Molecular Syndromology|January 7, 2016
Familial 1.3-Mb 11p15.5p15.4 Duplication in Three Generations Causing Silver-Russell and Beckwith-Wiedemann SyndromesMari-Anne Vals, Tiina Kahre, Pille Mee, et al.
European Journal of Medical Genetics|December 23, 2015
Two familial microduplications of 15q26.3 causing overgrowth and variable intellectual disability with normal copy number of IGF1RMelanie Leffler, Sanna Puusepp, Olga Žilina, et al.
Molecular Syndromology|January 7, 2016
The Diagnostic Utility of Single Long Contiguous Stretches of Homozygosity in Patients without Parental ConsanguinitySander Pajusalu, Olga Žilina, Maria Yakoreva, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 18, 2014
Monosomy 1p36 - a multifaceted and still enigmatic syndrome: four clinically diverse cases with shared white matter abnormalitiesEve Õiglane-Shlik, Sanna Puusepp, Inga Talvik, et al.
Scientific Reports|April 6, 2018
NIPTmer: rapid k-mer-based software package for detection of fetal aneuploidiesMartin Sauk, Olga Žilina, Ants Kurg, et al.
Prenatal Diagnosis|November 7, 2019
Olga Žilina, Kadri Rekker, Lauris Kaplinski, et al.
Nature Medicine|November 6, 2019
In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineagesMasoud Zamani Esteki, Triin Viltrop, Olga Tšuiko, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
European Journal of Medical Genetics|February 2, 2013
Patient with dup(5)(q35.2-q35.3) reciprocal to the common Sotos syndrome deletion and review of the literatureOlga Žilina, Tiia Reimand, Pille Tammur, et al.
BMC Genomics|September 18, 2015
Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genomeOlga Žilina, Marina Koltšina, Raivo Raid, et al.
Molecular Syndromology|September 6, 2018
A New Case of a Rare Combination of Temple Syndrome and Mosaic Trisomy 14 and a Literature ReviewMaria Yakoreva, Tiina Kahre, Sander Pajusalu, et al.
Molecular Syndromology|January 7, 2016
Familial 1.3-Mb 11p15.5p15.4 Duplication in Three Generations Causing Silver-Russell and Beckwith-Wiedemann SyndromesMari-Anne Vals, Tiina Kahre, Pille Mee, et al.
European Journal of Medical Genetics|December 23, 2015
Two familial microduplications of 15q26.3 causing overgrowth and variable intellectual disability with normal copy number of IGF1RMelanie Leffler, Sanna Puusepp, Olga Žilina, et al.
Molecular Syndromology|January 7, 2016
The Diagnostic Utility of Single Long Contiguous Stretches of Homozygosity in Patients without Parental ConsanguinitySander Pajusalu, Olga Žilina, Maria Yakoreva, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 18, 2014
Monosomy 1p36 - a multifaceted and still enigmatic syndrome: four clinically diverse cases with shared white matter abnormalitiesEve Õiglane-Shlik, Sanna Puusepp, Inga Talvik, et al.
Scientific Reports|April 6, 2018
NIPTmer: rapid k-mer-based software package for detection of fetal aneuploidiesMartin Sauk, Olga Žilina, Ants Kurg, et al.
Prenatal Diagnosis|November 7, 2019
Olga Žilina, Kadri Rekker, Lauris Kaplinski, et al.
Nature Medicine|November 6, 2019
In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineagesMasoud Zamani Esteki, Triin Viltrop, Olga Tšuiko, et al.
Pageof 1