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Maria A Zelenova

Showing results (1-10 of 9) with videos related to

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Molecular Cytogenetics|January 1, 2020
Laundering CNV data for candidate process prioritization in brain disordersMaria A Zelenova, Yuri B Yurov, Svetlana G Vorsanova, et al.
Current Genomics|April 3, 2018
Behavioral Variability and Somatic Mosaicism: A Cytogenomic HypothesisSvetlana G Vorsanova, Maria A Zelenova, Yuri B Yurov, et al.
Molecular Cytogenetics|October 20, 2015
Long contiguous stretches of homozygosity spanning shortly the imprinted loci are associated with intellectual disability, autism and/or epilepsyIvan Y Iourov, Svetlana G Vorsanova, Sergei A Korostelev, et al.
International Journal of Genomics|October 1, 2015
Genomic Copy Number Variation Affecting Genes Involved in the Cell Cycle Pathway: Implications for Somatic MosaicismIvan Y Iourov, Svetlana G Vorsanova, Maria A Zelenova, et al.
Current Genomics|April 3, 2018
4q21.2q21.3 Duplication: Molecular and Neuropsychological AspectsIvan Y Iourov, Maria A Zelenova, Svetlana G Vorsanova, et al.
Molecular Cytogenetics|January 1, 2013
Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomaliesIvan Y Iourov, Svetlana G Vorsanova, Oxana S Kurinnaia, et al.
International Journal of Molecular Sciences|November 11, 2020
The Cytogenomic "Theory of Everything": Chromohelkosis May Underlie Chromosomal Instability and Mosaicism in Disease and AgingIvan Y Iourov, Svetlana G Vorsanova, Yuri B Yurov, et al.
Molecular Cytogenetics|November 29, 2013
Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the diseaseIvan Y Iourov, Svetlana G Vorsanova, Victoria Y Voinova, et al.
Molecular Cytogenetics|January 4, 2023
Cytogenomic epileptologyIvan Y Iourov, Alexandr P Gerasimov, Maria A Zelenova, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Molecular Cytogenetics|January 1, 2020
Laundering CNV data for candidate process prioritization in brain disordersMaria A Zelenova, Yuri B Yurov, Svetlana G Vorsanova, et al.
Current Genomics|April 3, 2018
Behavioral Variability and Somatic Mosaicism: A Cytogenomic HypothesisSvetlana G Vorsanova, Maria A Zelenova, Yuri B Yurov, et al.
Molecular Cytogenetics|October 20, 2015
Long contiguous stretches of homozygosity spanning shortly the imprinted loci are associated with intellectual disability, autism and/or epilepsyIvan Y Iourov, Svetlana G Vorsanova, Sergei A Korostelev, et al.
International Journal of Genomics|October 1, 2015
Genomic Copy Number Variation Affecting Genes Involved in the Cell Cycle Pathway: Implications for Somatic MosaicismIvan Y Iourov, Svetlana G Vorsanova, Maria A Zelenova, et al.
Current Genomics|April 3, 2018
4q21.2q21.3 Duplication: Molecular and Neuropsychological AspectsIvan Y Iourov, Maria A Zelenova, Svetlana G Vorsanova, et al.
Molecular Cytogenetics|January 1, 2013
Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomaliesIvan Y Iourov, Svetlana G Vorsanova, Oxana S Kurinnaia, et al.
International Journal of Molecular Sciences|November 11, 2020
The Cytogenomic "Theory of Everything": Chromohelkosis May Underlie Chromosomal Instability and Mosaicism in Disease and AgingIvan Y Iourov, Svetlana G Vorsanova, Yuri B Yurov, et al.
Molecular Cytogenetics|November 29, 2013
Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the diseaseIvan Y Iourov, Svetlana G Vorsanova, Victoria Y Voinova, et al.
Molecular Cytogenetics|January 4, 2023
Cytogenomic epileptologyIvan Y Iourov, Alexandr P Gerasimov, Maria A Zelenova, et al.
Pageof 1