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Igor N Lebedev

Showing results (31-40 of 40) with videos related to

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Cytogenetic and Genome Research|May 31, 2022
Skewed X-Chromosome Inactivation as a Possible Marker of X-Linked CNV in Women with Pregnancy LossElizaveta A Fonova, Ekaterina N Tolmacheva, Anna A Kashevarova, et al.
Biomedicines|August 27, 2021
Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome SequencingIgor N Lebedev, Tatyana V Karamysheva, Eugeny A Elisaphenko, et al.
Molecular Cytogenetics|May 9, 2018
Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22Anna A Kashevarova, Elena O Belyaeva, Aleksandr M Nikonov, et al.
American Journal of Medical Genetics. Part A|September 24, 2018
A mosaic intragenic microduplication of LAMA1 and a constitutional 18p11.32 microduplication in a patient with keratosis pilaris and intellectual disabilityAnna A Kashevarova, Lyudmila P Nazarenko, Nikolay A Skryabin, et al.
Molecular Cytogenetics|February 22, 2025
Prevalence of CNVs on the X chromosome in patients with neurodevelopmental disordersEkaterina N Tolmacheva, Anna A Kashevarova, Elizaveta A Fonova, et al.
Molecular Neurobiology|January 13, 2018
Allele-Specific Biased Expression of the CNTN6 Gene in iPS Cell-Derived Neurons from a Patient with Intellectual Disability and 3p26.3 Microduplication Involving the CNTN6 GeneMaria M Gridina, Natalia M Matveeva, Veniamin S Fishman, et al.
Cytogenetic and Genome Research|April 13, 2021
Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental DelayStanislav A Vasilyev, Nikolay A Skryabin, Anna A Kashevarova, et al.
Nature Medicine|November 23, 2023
Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy lossRick Essers, Igor N Lebedev, Ants Kurg, et al.
Genome Medicine|May 7, 2025
Combining chromosome conformation capture and exome sequencing for simultaneous detection of structural and single-nucleotide variantsMaria Gridina, Timofey Lagunov, Polina Belokopytova, et al.
Molecular Psychiatry|January 22, 2019
Opening up new horizons for psychiatric genetics in the Russian Federation: moving toward a national consortiumOlga Yu Fedorenko, Vera E Golimbet, Svetlana А Ivanova, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Cytogenetic and Genome Research|May 31, 2022
Skewed X-Chromosome Inactivation as a Possible Marker of X-Linked CNV in Women with Pregnancy LossElizaveta A Fonova, Ekaterina N Tolmacheva, Anna A Kashevarova, et al.
Biomedicines|August 27, 2021
Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome SequencingIgor N Lebedev, Tatyana V Karamysheva, Eugeny A Elisaphenko, et al.
Molecular Cytogenetics|May 9, 2018
Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22Anna A Kashevarova, Elena O Belyaeva, Aleksandr M Nikonov, et al.
American Journal of Medical Genetics. Part A|September 24, 2018
A mosaic intragenic microduplication of LAMA1 and a constitutional 18p11.32 microduplication in a patient with keratosis pilaris and intellectual disabilityAnna A Kashevarova, Lyudmila P Nazarenko, Nikolay A Skryabin, et al.
Molecular Cytogenetics|February 22, 2025
Prevalence of CNVs on the X chromosome in patients with neurodevelopmental disordersEkaterina N Tolmacheva, Anna A Kashevarova, Elizaveta A Fonova, et al.
Molecular Neurobiology|January 13, 2018
Allele-Specific Biased Expression of the CNTN6 Gene in iPS Cell-Derived Neurons from a Patient with Intellectual Disability and 3p26.3 Microduplication Involving the CNTN6 GeneMaria M Gridina, Natalia M Matveeva, Veniamin S Fishman, et al.
Cytogenetic and Genome Research|April 13, 2021
Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental DelayStanislav A Vasilyev, Nikolay A Skryabin, Anna A Kashevarova, et al.
Nature Medicine|November 23, 2023
Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy lossRick Essers, Igor N Lebedev, Ants Kurg, et al.
Genome Medicine|May 7, 2025
Combining chromosome conformation capture and exome sequencing for simultaneous detection of structural and single-nucleotide variantsMaria Gridina, Timofey Lagunov, Polina Belokopytova, et al.
Molecular Psychiatry|January 22, 2019
Opening up new horizons for psychiatric genetics in the Russian Federation: moving toward a national consortiumOlga Yu Fedorenko, Vera E Golimbet, Svetlana А Ivanova, et al.
Pageof 4