I Iu Iurov - JoVE Visualize

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Genetika|November 11, 2010

[Molecular cytogenetic methods for studying interphase chromosomes in human brain cells]I Iu Iurov, S G Vorsanova, I V Solov'ev, et al.

Genetika|January 25, 2011

[Identification of candidate genes of autism on the basis of molecular cytogenetic and in silico studies of the genome organization of chromosomal regions involved in unbalanced rearrangements]I Iu Iurov, S G Vorsanova, E A Saprina, et al.

Gigiena I Sanitariia|December 22, 2011

[Original molecular cytogenetic approach to determining spontaneous chromosomal mutations in the interphase cells to evaluate the mutagenic activity of environmental factors]I Iu Iurov, S G Vorsanova, I V Solov'ev, et al.

Genetika|January 25, 2011

[Instability of chromosomes in human nerve cells (normal and with neuromental diseases)]Iu B Iurov, S G Vorsanova, I V Solov'ev, et al.

Vestnik Rossiiskoi Akademii Meditsinskikh Nauk|December 6, 2012

[Genomic instability in the brain: etiology, pathogenesis and new biological markers of psychiatric disorders]A S Tiganov, Iu B Iurov, S G Vorsanova, et al.

Klinicheskaia Laboratornaia Diagnostika|January 13, 2006

[Quantitative analysis of fluorescence in situ hybridization (FISH) signals for molecular cytogenetic diagnosis]I Iu Iurov, I V Solov'ev, V V Monakhov, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|October 1, 2013

[Genomic abnormalities in children with mental retardation and autism: the use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)]S G Vorsanova, I Iu Iurov, O S Kurinnaia, et al.

Tsitologiia I Genetika|May 11, 2005

[Molecular cytogenetic study of Robertsonian translocation 13;14 and Down syndrome in a 3-year-old infant]I Iu Iurov, S G Vorsanova, V V Monakhov, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|August 13, 2009

[Cytogenetic, molecular cytogenetic, clinical and genealogical study of mothers of children with autism: a search for family genetic markers of autistic disorders]S G Vorsanova, V Iu Voinova, I Iu Iurov, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|December 5, 2013

[Subchromosomal microdeletion identified by molecular karyotyping using DNA microarrays (array CGH) in Rett syndrome girls negative for MECP2 gene mutations]S G Vorsanova, I Iu Iurov, V Iu Voinova, et al.

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Showing results (1-10 of 17) with videos related to

Sort By:

Pageof 2

Genetika|November 11, 2010

[Molecular cytogenetic methods for studying interphase chromosomes in human brain cells]I Iu Iurov, S G Vorsanova, I V Solov'ev, et al.

Genetika|January 25, 2011

[Identification of candidate genes of autism on the basis of molecular cytogenetic and in silico studies of the genome organization of chromosomal regions involved in unbalanced rearrangements]I Iu Iurov, S G Vorsanova, E A Saprina, et al.

Gigiena I Sanitariia|December 22, 2011

[Original molecular cytogenetic approach to determining spontaneous chromosomal mutations in the interphase cells to evaluate the mutagenic activity of environmental factors]I Iu Iurov, S G Vorsanova, I V Solov'ev, et al.

Genetika|January 25, 2011

[Instability of chromosomes in human nerve cells (normal and with neuromental diseases)]Iu B Iurov, S G Vorsanova, I V Solov'ev, et al.

Vestnik Rossiiskoi Akademii Meditsinskikh Nauk|December 6, 2012

[Genomic instability in the brain: etiology, pathogenesis and new biological markers of psychiatric disorders]A S Tiganov, Iu B Iurov, S G Vorsanova, et al.

Klinicheskaia Laboratornaia Diagnostika|January 13, 2006

[Quantitative analysis of fluorescence in situ hybridization (FISH) signals for molecular cytogenetic diagnosis]I Iu Iurov, I V Solov'ev, V V Monakhov, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|October 1, 2013

[Genomic abnormalities in children with mental retardation and autism: the use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)]S G Vorsanova, I Iu Iurov, O S Kurinnaia, et al.

Tsitologiia I Genetika|May 11, 2005

[Molecular cytogenetic study of Robertsonian translocation 13;14 and Down syndrome in a 3-year-old infant]I Iu Iurov, S G Vorsanova, V V Monakhov, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|August 13, 2009

[Cytogenetic, molecular cytogenetic, clinical and genealogical study of mothers of children with autism: a search for family genetic markers of autistic disorders]S G Vorsanova, V Iu Voinova, I Iu Iurov, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|December 5, 2013

[Subchromosomal microdeletion identified by molecular karyotyping using DNA microarrays (array CGH) in Rett syndrome girls negative for MECP2 gene mutations]S G Vorsanova, I Iu Iurov, V Iu Voinova, et al.

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