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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.

Klinicheskaia Laboratornaia Diagnostika|October 14, 2000

[Development of an original computer program FISHMet: use for molecular cytogenetic diagnosis and genome mapping by fluorescent in situ hybridization (FISH)]Iu B Iurov, I A Khazatskiĭ, V A Akindinov, 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|January 1, 1996

[The search for a mutation in the gene coding the beta-amyloid protein precursor gene in patients with Alzheimer-type dementias]V E Golimbet, I V Ovchinnikov, N I Voskresenskaia, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|March 10, 2000

[Serotonin receptor gene allele polymorphism (5HTR2A) and clinical pathogenetic characteristics in patients with schizophrenia and schizophrenia spectrum disorders]V E Golimbet, K K Manandian, L I Abramova, 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.

Klinicheskaia Laboratornaia Diagnostika|January 13, 2006

[Diagnosis of numerical chromosomal aberrations in the cells of spontaneous abortions by multicolor fluorescence in situ hybridization (MFISH)]S G Vorsanova, A D Kolotiĭ, I Iu Iurov, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|July 18, 2006

[Variations of heterochromatic chromosomal regions and chromosome abnormalities in children with autism: identification of genetic markers in autistic spectrum disorders]S G Vorsanova, I Iu Iurov, I A Demidova, et al.

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Showing results (31-40 of 50) with videos related to

Sort By:

Pageof 5

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.

Klinicheskaia Laboratornaia Diagnostika|October 14, 2000

[Development of an original computer program FISHMet: use for molecular cytogenetic diagnosis and genome mapping by fluorescent in situ hybridization (FISH)]Iu B Iurov, I A Khazatskiĭ, V A Akindinov, 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|January 1, 1996

[The search for a mutation in the gene coding the beta-amyloid protein precursor gene in patients with Alzheimer-type dementias]V E Golimbet, I V Ovchinnikov, N I Voskresenskaia, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|March 10, 2000

[Serotonin receptor gene allele polymorphism (5HTR2A) and clinical pathogenetic characteristics in patients with schizophrenia and schizophrenia spectrum disorders]V E Golimbet, K K Manandian, L I Abramova, 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.

Klinicheskaia Laboratornaia Diagnostika|January 13, 2006

[Diagnosis of numerical chromosomal aberrations in the cells of spontaneous abortions by multicolor fluorescence in situ hybridization (MFISH)]S G Vorsanova, A D Kolotiĭ, I Iu Iurov, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|July 18, 2006

[Variations of heterochromatic chromosomal regions and chromosome abnormalities in children with autism: identification of genetic markers in autistic spectrum disorders]S G Vorsanova, I Iu Iurov, I A Demidova, et al.

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