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Molecular Human Reproduction|September 1, 1996
Rapid chromosomal analysis of germ-line cells by FISH: an investigation of an infertile male with large-headed spermatozoaY B Yurov, M J Saias, S G Vorsanova, 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|January 17, 2017
[Genomic instability in the brain: chromosomal mosaicism in schizophrenia]Y B Yurov, S G Vorsanova, I A Demidova, 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.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|November 4, 2015
[Clinical and genetic characteristics of the X chromosome distal long arm microduplications encompassing the MECP2 gene]V Yu Voinova, S G Vorsanova, Yu B Yurov, et al.
Neuroscience and Behavioral Physiology|July 28, 2007
Variability in the heterochromatin regions of the chromosomes and chromosomal anomalies in children with autism: identification of genetic markers of autistic spectrum disordersS G Vorsanova, I Yu Yurov, I A Demidova, 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.
Genetika|March 30, 1999
[Study of alpha-satellite DNA in cosmid libraries, specific for chromosomes 13, 21, and 22, using fluorescence in situ hybridization]I V Solov'ev, Iu B Iurov, S G Vorsanova, et al.
Tsitologiia I Genetika|February 18, 2005
[X chromosome inactivation pattern in elderly women over 70 years of age]I Iu Iurov, L Willard, S G Vorsanova, et al.
Tsitologiia I Genetika|April 22, 2004
[A case of deletion of the short arm of the chromosome 21 (21p-) (christchurch chromosome) discovered prenatally:clinical and cytogenetic data]L V Tavokina, S G Vorsanova, V D Zukin, et al.
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