S G Vorsanova - JoVE Visualize

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Human Genetics|February 1, 1986

18p- syndrome: an unusual case and diagnosis by in situ hybridization with chromosome 18-specific alphoid DNA sequenceS G Vorsanova, Y B Yurov, I A Alexandrov, et al.

Molekuliarnaia Biologiia|February 10, 2021

[Causes and Consequences of Genome Instability in Psychiatric and Neurodegenerative Diseases]I Y Iourov, S G Vorsanova, O S Kurinnaia, et al.

Tsitologiia I Genetika|March 28, 2007

Chimerism and multiple numerical chromosome imbalances in a spontaneously aborted fetusS G Vorsanova, I Y Iourov, I A Demidova, et al.

Tsitologiia I Genetika|May 1, 1994

Identification of marker chromosomes by in situ hybridization technique using alpha and "classical" satellite DNA probes with relative chromosomal specificityS G Vorsanova, Y B Yurov, I Passarge, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|July 19, 2019

[Epigenomic variations manifesting as a loss of heterozygosity affecting imprinted genes represent a molecular mechanism of autism spectrum disorders and intellectual disability in children]I Y Iourov, S G Vorsanova, M A Zelenova, et al.

Tsitologiia I Genetika|September 1, 1995

[An analysis of human marker chromosomes originating from chromosome 21 by using in situ hybridization]T E Zerova, E V Baronova, N G Gorovenko, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|June 2, 1998

[Cytogenetic and molecular genetic diagnostics of Rett syndrome in children]S G Vorsanova, I A Demidova, V Iu Ulas, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|August 9, 2016

[Structural variations of the genome in autistic spectrum disorders with intellectual disability]I Yu Iourov, S G Vorsanova, S A Korostelev, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|March 19, 2014

[The use of molecular cytogenetic and cytogenetic techniques for the diagnosis of Prader-Willi and Angelman syndrome]I Y Iourov, S G Vorsanova, O S Kurinnaaya, et al.

Human Genetics|September 1, 1990

Preliminary results on the frequency of the delta F508 mutation in cystic fibrosis patients from the USSRP Ronchetto, M Devoto, A Puliti, et al.

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Showing results (51-60 of 79) with videos related to

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Human Genetics|February 1, 1986

18p- syndrome: an unusual case and diagnosis by in situ hybridization with chromosome 18-specific alphoid DNA sequenceS G Vorsanova, Y B Yurov, I A Alexandrov, et al.

Molekuliarnaia Biologiia|February 10, 2021

[Causes and Consequences of Genome Instability in Psychiatric and Neurodegenerative Diseases]I Y Iourov, S G Vorsanova, O S Kurinnaia, et al.

Tsitologiia I Genetika|March 28, 2007

Chimerism and multiple numerical chromosome imbalances in a spontaneously aborted fetusS G Vorsanova, I Y Iourov, I A Demidova, et al.

Tsitologiia I Genetika|May 1, 1994

Identification of marker chromosomes by in situ hybridization technique using alpha and "classical" satellite DNA probes with relative chromosomal specificityS G Vorsanova, Y B Yurov, I Passarge, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|July 19, 2019

[Epigenomic variations manifesting as a loss of heterozygosity affecting imprinted genes represent a molecular mechanism of autism spectrum disorders and intellectual disability in children]I Y Iourov, S G Vorsanova, M A Zelenova, et al.

Tsitologiia I Genetika|September 1, 1995

[An analysis of human marker chromosomes originating from chromosome 21 by using in situ hybridization]T E Zerova, E V Baronova, N G Gorovenko, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|June 2, 1998

[Cytogenetic and molecular genetic diagnostics of Rett syndrome in children]S G Vorsanova, I A Demidova, V Iu Ulas, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|August 9, 2016

[Structural variations of the genome in autistic spectrum disorders with intellectual disability]I Yu Iourov, S G Vorsanova, S A Korostelev, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|March 19, 2014

[The use of molecular cytogenetic and cytogenetic techniques for the diagnosis of Prader-Willi and Angelman syndrome]I Y Iourov, S G Vorsanova, O S Kurinnaaya, et al.

Human Genetics|September 1, 1990

Preliminary results on the frequency of the delta F508 mutation in cystic fibrosis patients from the USSRP Ronchetto, M Devoto, A Puliti, et al.

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