Vorsanova SG - Search Results

1

Chromosome Instability in the Neurodegenerating Brain.

Yurov YB, Vorsanova SG, Iourov IY. Yurov YB, et al. Among authors: vorsanova sg. Front Genet. 2019 Sep 20;10:892. doi: 10.3389/fgene.2019.00892. eCollection 2019. Front Genet. 2019. PMID: 31616475 Free PMC article. No abstract available.

2

Translocation t(1;17)(q12;q25) with a clinical picture like of a proximal deletion of 1q: identification by in situ hybridization with chromosome 1-specific satellite DNA probes.

Vorsanova SG, Yurov YB, Kurbatov MB, Kazantzeva LZ. Vorsanova SG, et al. Hum Genet. 1990 Dec;86(2):173-4. doi: 10.1007/BF00197700. Hum Genet. 1990. PMID: 2265830

3

18p- syndrome: an unusual case and diagnosis by in situ hybridization with chromosome 18-specific alphoid DNA sequence.

Vorsanova SG, Yurov YB, Alexandrov IA, Demidova IA, Mitkevich SP, Tirskaia AF. Vorsanova SG, et al. Hum Genet. 1986 Feb;72(2):185-7. doi: 10.1007/BF00283945. Hum Genet. 1986. PMID: 3753696

4

Prenatal diagnosis of trisomy 21 using interphase fluorescence in situ hybridization of post-replicated cells with site-specific cosmid and cosmid contig probes.

Soloviev IV, Yurov YB, Vorsanova SG, Fayet F, Roizes G, Malet P. Soloviev IV, et al. Among authors: vorsanova sg. Prenat Diagn. 1995 Mar;15(3):237-48. doi: 10.1002/pd.1970150307. Prenat Diagn. 1995. PMID: 7784382

5

Rapid identification of marker chromosomes by in situ hybridization under different stringency conditions.

Vorsanova SG, Yurov YB, Soloviev IV, Demidova IA, Malet P. Vorsanova SG, et al. Anal Cell Pathol. 1994 Oct;7(3):251-8. Anal Cell Pathol. 1994. PMID: 7848878

6

Analysis of pericentromeric chromosome 21 specific YAC clones by FISH: identification of new markers for molecular-cytogenetic application.

Yurov YB, Laurent AM, Marcais B, Vorsanova SG, Roizes G. Yurov YB, et al. Among authors: vorsanova sg. Hum Genet. 1995 Mar;95(3):287-92. doi: 10.1007/BF00225195. Hum Genet. 1995. PMID: 7868120

7

Identification of marker chromosomes by in situ hybridization technique using alpha and "classical" satellite DNA probes with relative chromosomal specificity.

Vorsanova SG, Yurov YB, Passarge I, Schmidt A, Zerova TE, Demidova IA, Buzhiyevskaya TI. Vorsanova SG, et al. Tsitol Genet. 1994 May-Jun;28(3):67-70. Tsitol Genet. 1994. PMID: 7974787

8

High resolution multicolor fluorescence in situ hybridization using cyanine and fluorescein dyes: rapid chromosome identification by directly fluorescently labeled alphoid DNA probes.

Yurov YB, Soloviev IV, Vorsanova SG, Marcais B, Roizes G, Lewis R. Yurov YB, et al. Among authors: vorsanova sg. Hum Genet. 1996 Mar;97(3):390-8. doi: 10.1007/BF02185780. Hum Genet. 1996. PMID: 8786090

9

Rapid chromosomal analysis of germ-line cells by FISH: an investigation of an infertile male with large-headed spermatozoa.

Yurov YB, Saias MJ, Vorsanova SG, Erny R, Soloviev IV, Sharonin VO, Guichaoua MR, Luciani JM. Yurov YB, et al. Among authors: vorsanova sg. Mol Hum Reprod. 1996 Sep;2(9):665-8. doi: 10.1093/molehr/2.9.665. Mol Hum Reprod. 1996. PMID: 9239680

10

Analysis of alphoid DNA variation and kinetochore size in human chromosome 21: evidence against pathological significance of alphoid satellite DNA diminutions.

Marzais B, Vorsanova SG, Roizes G, Yurov YB. Marzais B, et al. Among authors: vorsanova sg. Tsitol Genet. 1999 Jan-Feb;33(1):25-31. Tsitol Genet. 1999. PMID: 10330695

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