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Svetlana Vorsanova

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Co-Publications
Name
34
Yurov, Yuri
28
Iourov, Ivan
25
Iurov, IuB
24
Demidova, Irina
14
Kolotii, Alexei
12
Soloviev, Ilia
10
Solov'ev, IV
10
Beresheva, Alphia
10
Monakhov, Viktor
9
Iurov, IIu
7
Kravets, Viktor
7
Liehr, Thomas
4
Kirillova, Elena
3
Roizes, G
3
Ulas, VIu

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Publications

TOP 3
Iourov Ivan Y; Vorsanova Svetlana G; Liehr Thomas; Kolotii Alexei D; Yurov Yuri B
Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain.
Iourov Ivan Y; Vorsanova Svetlana G; Liehr Thomas; Yurov Yuri B
Aneuploidy in the normal, Alzheimer's disease and ataxia-telangiectasia brain: differential expression and pathological meaning.
Iourov Ivan Y; Vorsanova Svetlana G; Yurov Yuri B
Developmental neural chromosome instability as a possible cause of childhood brain cancers.

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All Publications

2009: Iourov Ivan Y; Vorsanova Svetlana G; Liehr Thomas; Kolotii Alexei D; Yurov Yuri B
Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain.
Human molecular genetics 2009;18(14):2656-69.
2009: Iourov Ivan Y; Vorsanova Svetlana G; Liehr Thomas; Yurov Yuri B
Aneuploidy in the normal, Alzheimer's disease and ataxia-telangiectasia brain: differential expression and pathological meaning.
Neurobiology of disease 2009;34(2):212-20.
2009: Iourov Ivan Y; Vorsanova Svetlana G; Yurov Yuri B
Developmental neural chromosome instability as a possible cause of childhood brain cancers.
Medical hypotheses 2009;72(5):615-6.
2008: Iourov I Y; Vorsanova S G; Yurov Y B
Molecular cytogenetics and cytogenomics of brain diseases.
Current genomics 2008;9(7):452-65.
2008: Vorsanova Svetlana G; Yurov Yuri B; Iourov Ivan Y
Maternal smoking as a cause of mosaic aneuploidy in spontaneous abortions.
Medical hypotheses 2008;71(4):607.
2008: Iourov I Y; Vorsanova S G; Yurov Y B
Fluorescence intensity profiles of in situ hybridization signals depict genome architecture within human interphase nuclei.
T?Sitologii?a i genetika 2008;42(5):3-8.
2008: Yurov Yuri B; Iourov Ivan Y; Vorsanova Svetlana G; Demidova Irina A; Kravetz Viktor S; Beresheva Alphia K; Kolotii Alexei D; Monakchov Viktor V; Uranova Natalia A; Vostrikov Viktor M; Soloviev Ilia V; Liehr Thomas
The schizophrenia brain exhibits low-level aneuploidy involving chromosome 1.
Schizophrenia research 2008;98(1-3):139-47.
2008: Iourov Ivan Y; Vorsanova Svetlana G; Yurov Yuri B
Chromosomal mosaicism goes global.
Molecular Cytogenetics 2008;1():26.
2008: Iourov I Y; Vorsanova S G; Liehr T; Monakhov V V; Soloviev I V; Yurov Y B
Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia.
Cytogenetic and genome research 2008;121(3-4):302-6.
2008: Vorsanova Svetlana G; Iourov Ivan Y; Voinova-Ulas Victoria Y; Weise Anja; Monakhov Victor V; Kolotii Alexei D; Soloviev Ilia V; Novikov Petr V; Yurov Yuri B; Liehr Thomas
Partial monosomy 7q34-qter and 21pter-q22.13 due to cryptic unbalanced translocation t(7;21) but not monosomy of the whole chromosome 21: a case report plus review of the literature.
Molecular Cytogenetics 2008;1(1):13.
2008: Yurov Yuri B; Liehr Thomas; Shaffer Lisa G; Iourov Ivan Y; Vorsanova Svetlana G
A new open access journal for a rapidly evolving biomedical field: introducing Molecular Cytogenetics.
Molecular Cytogenetics 2008;1(1):1.
2008: Iourov Ivan Y; Yurov Yuri B; Vorsanova Svetlana G
Mosaic X chromosome aneuploidy can help to explain the male-to-female ratio in autism.
Medical hypotheses 2008;70(2):456.
2007: Iourov Ivan Y; Liehr Thomas; Vorsanova Svetlana G; Yurov Yuri B
Interphase chromosome-specific multicolor banding (ICS-MCB): a new tool for analysis of interphase chromosomes in their integrity.
Biomolecular engineering 2007;24(4):415-7.
2007: Yurov Y B; Vorsanova S G; Iourov I Y; Demidova I A; Beresheva A K; Kravetz V S; Monakhov V V; Kolotii A D; Voinova-Ulas V Y; Gorbachevskaya N L
Unexplained autism is frequently associated with low-level mosaic aneuploidy.
Journal of medical genetics 2007;44(8):521-5.
2007: Vorsanova S G; Yurov I Yu; Demidova I A; Voinova-Ulas V Yu; Kravets V S; Solov'ev I V; Gorbachevskaya N L; Yurov Yu B
Variability in the heterochromatin regions of the chromosomes and chromosomal anomalies in children with autism: identification of genetic markers of autistic spectrum disorders.
Neuroscience and behavioral physiology 2007;37(6):553-8.
2007: Yurov Yuri B; Iourov Ivan Y; Vorsanova Svetlana G; Liehr Thomas; Kolotii Alexei D; Kutsev Sergei I; Pellestor Franck; Beresheva Alfia K; Demidova Irina A; Kravets Viktor S; Monakhov Viktor V; Soloviev Ilia V
Aneuploidy and confined chromosomal mosaicism in the developing human brain.
PloS one 2007;2(6):e558.
2007: Iourov Ivan Y; Vorsanova Svetlana G; Yurov Yuri B
Ataxia telangiectasia paradox can be explained by chromosome instability at the subtissue level.
Medical hypotheses 2007;68(3):716.
2006: Iourov Ivan Y; Vorsanova Svetlana G; Kirillova Elena A; Yurov Yuri B
First case of del(1)(p36.2p33) in a fetus delivered stillborn.
Prenatal diagnosis 2006;26(11):1092-3.
2006: Vorsanova S G; Iourov I Y; Demidova I A; Kirillova E A; Soloviev I V; Yurov Y B
Chimerism and multiple numerical chromosome imbalances in a spontaneously aborted fetus.
T?Sitologii?a i genetika 2006;40(5):28-30.
2006: Vorsanova S G; Iourov I Y; Demidova I A; Kolotii A D; Soloviev I V; Yurov Y B
Pericentric inversion inv(7)(p11q21.1): report on two cases and genotype-phenotype correlations.
T?Sitologii?a i genetika 2006;40(3):45-8.
2006: Vel'tishchev Iu E; Tsaregorodtsev A D; Novikov P V; Vorsanova S G
[The use of modern diagnostic and preventive technologies in children with hereditary and congenital intellectual developmental disorders]
Vestnik Rossiiskoi akademii meditsinskikh nauk / Rossiiskaia akademiia meditsinskikh nauk 2006;(9-10):11-8.
2006: Iourov Ivan Y; Vorsanova Svetlana G; Pellestor Franck; Yurov Yuri B
Brain tissue preparations for chromosomal PRINS labeling.
Methods in molecular biology (Clifton, N.J.) 2006;334():123-32.
2006: Vorsanova S G; Iurov I Iu; Demidova I A; Voinova-Ulas V Iu; Kravets V S; Solov'ev I V; Gorbachevskaia N L; Iurov Iu B
[Variations of heterochromatic chromosomal regions and chromosome abnormalities in children with autism: identification of genetic markers in autistic spectrum disorders]
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova / Ministerstvo zdravookhraneniia i meditsinskoi promyshlennosti Rossiiskoi Federatsii, Vserossiiskoe obshchestvo nevrologov [i] Vserossiiskoe obshchestvo psikhiatrov 2006;106(6):52-7.
2006: Iourov Ivan Y; Vorsanova Svetlana G; Yurov Yuri B
Chromosomal variation in mammalian neuronal cells: known facts and attractive hypotheses.
International review of cytology 2006;249():143-91.
2006: Iourov I Y; Liehr T; Vorsanova S G; Kolotii A D; Yurov Y B
Visualization of interphase chromosomes in postmitotic cells of the human brain by multicolour banding (MCB).
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2006;14(3):223-9.
2006: Iurov I Iu; Vorsanova S G; Iurov Iu B
[Chromosome abnormalities in schizophrenia]
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova / Ministerstvo zdravookhraneniia i meditsinskoi promyshlennosti Rossiiskoi Federatsii, Vserossiiskoe obshchestvo nevrologov [i] Vserossiiskoe obshchestvo psikhiatrov 2006;106(3):75-82.
2005: Iurov I Iu; Solov'ev I V; Monakhov V V; Vorsanova S G; Iurov Iu B
[Quantitative analysis of fluorescence in situ hybridization (FISH) signals for molecular cytogenetic diagnosis]
Klinicheskaia laboratornaia diagnostika 2005;(11):33-6.
2005: Vorsanova S G; Kolotii A D; Iurov I Iu; Kirillova E A; Monakhov V V; Beresheva A K; Solov'ev I V; Iurov Iu B
[Diagnosis of numerical chromosomal aberrations in the cells of spontaneous abortions by multicolor fluorescence in situ hybridization (MFISH)]
Klinicheskaia laboratornaia diagnostika 2005;(11):30-2.
2005: Vorsanova S G; Iourov I Y; Beresheva A K; Demidova I A; Monakhov V V; Kravets V S; Bartseva O B; Goyko E A; Soloviev I V; Yurov Y B
Non-disjunction of chromosome 21, alphoid DNA variation, and sociogenetic features of Down syndrome.
T?Sitologii?a i genetika 2005;39(6):30-6.
2005: Iourov Ivan Y; Soloviev Ilia V; Vorsanova Svetlana G; Monakhov Viktor V; Yurov Yuri B
An approach for quantitative assessment of fluorescence in situ hybridization (FISH) signals for applied human molecular cytogenetics.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):401-8.
2005: Yurov Yuri B; Iourov Ivan Y; Monakhov Viktor V; Soloviev Ilia V; Vostrikov Viktor M; Vorsanova Svetlana G
The variation of aneuploidy frequency in the developing and adult human brain revealed by an interphase FISH study.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):385-90.
2005: Vorsanova Svetlana G; Kolotii Alexei D; Iourov Ivan Y; Monakhov Viktor V; Kirillova Elena A; Soloviev Ilia V; Yurov Yuri B
Evidence for high frequency of chromosomal mosaicism in spontaneous abortions revealed by interphase FISH analysis.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):375-80.
2005: Iurov I Iu; Vorsanova S G; Voinova-Ulas V Iu; Villard L; Demidova I A; Giunti L; Guivabyccu-Uzielli M L; Budilov A V; Beresheva A K; Novikov P V; Iurov Iu V
[Epigenetic study of Rett's syndrome as an adequate model for autistic disorders]
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova / Ministerstvo zdravookhraneniia i meditsinskoi promyshlennosti Rossiiskoi Federatsii, Vserossiiskoe obshchestvo nevrologov [i] Vserossiiskoe obshchestvo psikhiatrov 2005;105(7):4-11.
2004: Iurov I Iu; Vorsanova S G; Monakhov V V; Beresheva A K; Solov'ev I V; Iurov Iu B
[Molecular cytogenetic study of Robertsonian translocation 13;14 and Down syndrome in a 3-year-old infant]
T?Sitologii?a i genetika 2004;38(6):54-9.
2004: Iurov I Iu; Willard L; Vorsanova S G; Demidova I A; Goiko E A; Shal'nova S A; Shkol'nikova M A; Olfer'ev A M; Iurov Iu B
[X chromosome inactivation pattern in elderly women over 70 years of age]
T?Sitologii?a i genetika 2004;38(4):49-54.
2004: Tavokina L V; Vorsanova S G; Zukin V D; Sopko N I; Zinchenko V M; Veselovskii V V; Bychkova A M; Nikitchina T V; Iurov Iu B
[A case of deletion of the short arm of the chromosome 21 (21p-) (christchurch chromosome) discovered prenatally:clinical and cytogenetic data]
T?Sitologii?a i genetika 2004;38(1):26-30.
2004: Iurov I Iu; Vorsanova S G; Iurov Iu B
[Nervous and mental diseases in boys and mutations in MECP2 gene]
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova / Ministerstvo zdravookhraneniia i meditsinskoi promyshlennosti Rossiiskoi Federatsii, Vserossiiskoe obshchestvo nevrologov [i] Vserossiiskoe obshchestvo psikhiatrov 2004;104(10):73-80.
2002: Vorsanova S G; Yurov Yu B; Brusquant D; Carles E; Roizes G
Two new cases of the Christchurch (Ch1) chromosome 21: evidence for clinical consequences of de novo deletion 21P-.
T?Sitologii?a i genetika 2002;36(1):46-9.
2002: Vorsanova S G; Ulas V Iu; Iurov Iu B; Giovanucci-Uzielli M L; Demidova I A; Gianti L; Villard L; Iurov I Iu; Beresheva A K; Novikov P V
[Genotype-phenotype correlations in Rett syndrome: the study of Russian cohort of patients]
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova / Ministerstvo zdravookhraneniia i meditsinskoi promyshlennosti Rossiiskoi Federatsii, Vserossiiskoe obshchestvo nevrologov [i] Vserossiiskoe obshchestvo psikhiatrov 2002;102(10):23-9.
2001: Yurov Y B; Vorsanova S G; Kolotii A D; Iourov I Y
Molecular-cytogenetic investigation of skewed chromosome X inactivation in Rett syndrome.
Brain & development 2001;23 Suppl 1():S214-7.
2001: Vorsanova S G; Yurov Y B; Ulas V Y; Demidova I A; Sharonin V O; Kolotii A D; Gorbatchevskaia N L; Beresheva A K; Soloviev I V
Cytogenetic and molecular-cytogenetic studies of Rett syndrome (RTT): a retrospective analysis of a Russian cohort of RTT patients (the investigation of 57 girls and three boys).
Brain & development 2001;23 Suppl 1():S196-201.
2001: Vorsanova S G; Yurov Y B; Kolotii A D; Soloviev I V
FISH analysis of replication and transcription of chromosome X loci: new approach for genetic analysis of Rett syndrome.
Brain & development 2001;23 Suppl 1():S191-5.
2001: Yurov Y B; Vostrikov V M; Vorsanova S G; Monakhov V V; Iourov I Y
Multicolor fluorescent in situ hybridization on post-mortem brain in schizophrenia as an approach for identification of low-level chromosomal aneuploidy in neuropsychiatric diseases.
Brain & development 2001;23 Suppl 1():S186-90.
2001: Gratchev V V; Bashina V M; Klushnik T P; Ulas V U; Gorbachevskaya N L; Vorsanova S G
Clinical, neurophysiological and immunological correlations in classical Rett syndrome.
Brain & development 2001;23 Suppl 1():S108-12.
2001: Iurov Iu B; Vorsanova S G
[Molecular cytogenetic studies of chromosomal abnormalities and disorders in nervous and mental diseases: search for biological markers for diagnosis]
Vestnik Rossiiskoi akademii meditsinskikh nauk / Rossiiskaia akademiia meditsinskikh nauk 2001;(7):26-31.
2000: Vorsanova S G; Yurov Y B; Kolotii A D; Demidova I A; Novikova I M
16q subtelomeric deletion in proband with congenital malformations and mental retardation.
T?Sitologii?a i genetika 2000;34(6):72-4.
2000: Vorsanova S G; Iurov Iu B; Solov'ev I V; Demidova I A; Sharonin V O; Male R; Zhiollant M; Beresheva A K; Kolotii A D; Kravets V S; Ruazes Zh
[Current methods of molecular cytogenetics in pre- and postnatal diagnosis of chromosome aberrations]
Klinicheskaia laboratornaia diagnostika 2000;(8):36-9.
2000: Iurov Iu B; Khazatskii I A; Akindinov V A; Dovgilov L V; Kobrinskii B A; Vorsanova S G
[Development of an original computer program FISHMet: use for molecular cytogenetic diagnosis and genome mapping by fluorescent in situ hybridization (FISH)]
Klinicheskaia laboratornaia diagnostika 2000;(8):34-6.
1999: Marzais B; Vorsanova S G; Roizes G; Yurov Y B
Analysis of alphoid DNA variation and kinetochore size in human chromosome 21: evidence against pathological significance of alphoid satellite DNA diminutions.
T?Sitologii?a i genetika 1999;33(1):25-31.
1999: Vorsanova S G; Iurov Iu B
[Molecular cytogenetic pre- and postnatal diagnosis of chromosomal abnormalities]
Vestnik Rossiiskoi akademii meditsinskikh nauk / Rossiiskaia akademiia meditsinskikh nauk 1999;(11):12-5.
1999: Vorsanova S G; Ulas V Iu; Demidova I A; Kravets V S; Iurov Iu B
[Contemporary views on Rett's syndrome: clinical, cytogenetic and molecular studies]
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova / Ministerstvo zdravookhraneniia i meditsinskoi promyshlennosti Rossiiskoi Federatsii, Vserossiiskoe obshchestvo nevrologov [i] Vserossiiskoe obshchestvo psikhiatrov 1999;99(3):61-9.
1998: Solov'ev I V; Iurov Iu B; Vorsanova S G; Marcais B; Rogaev E I; Kapanadze B I; Brodianskii V M; Iankovskii N K; Roizes G
[Study of alpha-satellite DNA in cosmid libraries, specific for chromosomes 13, 21, and 22, using fluorescence in situ hybridization]
Genetika 1998;34(11):1470-9.
1998: Soloviev I V; Yurov YuD; Vorsanova S G; Malet P; Zerova T E; Buzhievskaya T I
Double color in situ hybridization of alpha-satellite chromosome 13, 21 specific cosmid clones for a rapid screening of their specificity.
T?Sitologii?a i genetika 1998;32(4):60-4.
1998: Vorsanova S G; Vekhova I V; Demidova I A; Iurov Iu B
[Mental retardation syndrome due to fragile X chromosome: diagnostic and genetic problems]
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova / Ministerstvo zdravookhraneniia i meditsinskoi promyshlennosti Rossiiskoi Federatsii, Vserossiiskoe obshchestvo nevrologov [i] Vserossiiskoe obshchestvo psikhiatrov 1998;98(9):54-63.
1998: Vorsanova S G; Vekhova N V; Solov'ev I V; Kazantseva L Z; Troitskaia L A; Iurov Iu B
[A familial case of mental retardation syndrome linked to fragile X chromosome]
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova / Ministerstvo zdravookhraneniia i meditsinskoi promyshlennosti Rossiiskoi Federatsii, Vserossiiskoe obshchestvo nevrologov [i] Vserossiiskoe obshchestvo psikhiatrov 1998;98(5):47-9.
1998: Vorsanova S G; Demidova I A; Ulas V Iu; Solov'ev I V; Kravets V S; Kazantseva L Z; Iurov Iu B
[Cytogenetic and molecular genetic diagnostics of Rett syndrome in children]
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova / Ministerstvo zdravookhraneniia i meditsinskoi promyshlennosti Rossiiskoi Federatsii, Vserossiiskoe obshchestvo nevrologov [i] Vserossiiskoe obshchestvo psikhiatrov 1998;98(4):53-6.
1996: Vorsanova S G; Demidova I A; Ulas VYu; Soloviev I V; Kazantzeva L Z; Yurov YuB
Cytogenetic and molecular-cytogenetic investigation of Rett syndrome: analysis of 31 cases.
Neuroreport 1996;8(1):187-9.
1996: Yurov Y B; Saias M J; Vorsanova S G; Erny R; Soloviev I V; Sharonin V O; Guichaoua M R; Luciani J M
Rapid chromosomal analysis of germ-line cells by FISH: an investigation of an infertile male with large-headed spermatozoa.
Molecular human reproduction 1996;2(9):665-8.
1996: Yurov Y B; Soloviev I V; Vorsanova S G; Marcais B; Roizes G; Lewis R
High resolution multicolor fluorescence in situ hybridization using cyanine and fluorescein dyes: rapid chromosome identification by directly fluorescently labeled alphoid DNA probes.
Human genetics 1996;97(3):390-8.
1995: Zerova T E; Baronova E V; Gorovenko N G; Koblianskaia G N; Buzhievskaia T I; Vorsanova S G; Iurov Iu B
[An analysis of human marker chromosomes originating from chromosome 21 by using in situ hybridization]
T?Sitologii?a i genetika 1995;29(5):41-8.
1995: Yurov Y B; Laurent A M; Marcais B; Vorsanova S G; Roizes G
Analysis of pericentromeric chromosome 21 specific YAC clones by FISH: identification of new markers for molecular-cytogenetic application.
Human genetics 1995;95(3):287-92.
1995: Soloviev I V; Yurov Y B; Vorsanova S G; Fayet F; Roizes G; Malet P
Prenatal diagnosis of trisomy 21 using interphase fluorescence in situ hybridization of post-replicated cells with site-specific cosmid and cosmid contig probes.
Prenatal diagnosis 1995;15(3):237-48.
1994: Vorsanova S G; Yurov Y B; Soloviev I V; Demidova I A; Malet P
Rapid identification of marker chromosomes by in situ hybridization under different stringency conditions.
Analytical cellular pathology : the journal of the European Society for Analytical Cellular Pathology 1994;7(3):251-8.
1994: Zerova-Liubimova T E; Buzhievskaia T I; Vorsanova S G; Iurov Iu B
[A review of the data from cytogenetic and molecular cytogenetic research on human supernumerary minichromosomes]
T?Sitologii?a i genetika 1994;28(5):81-8.
1994: Vorsanova S G; Yurov Y B; Passarge I; Schmidt A; Zerova T E; Demidova I A; Buzhiyevskaya T I
Identification of marker chromosomes by in situ hybridization technique using alpha and "classical" satellite DNA probes with relative chromosomal specificity.
T?Sitologii?a i genetika 1994;28(3):67-70.
1993: Vorsanova S G; Iurov Iu B; Demidova I A; Vekhova N V
[Chromosomal anomalies in children with undifferentiated forms of metal retardation based on molecular cytogenetic research data]
T?Sitologii?a i genetika 1993;27(3):72-8.
1991: Vorsanova S G; Iurov Iu B; Deriagin G V; Solov'ev I V; Bytenskaia G A
[Method of diagnosing aneuploidies using in situ hybridization: analysis of interphase nuclei]
Biulleten' eksperimental'noi biologii i meditsiny 1991;112(10):413-5.
1990: Vorsanova S G; Yurov Y B; Kurbatov M B; Kazantzeva L Z
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.
Human genetics 1990;86(2):173-4.
1989: Vorsanova S G; Iurov Iu B; Aleksandrov I A; Demidova I A; Mitkevich S P
[Molecular-cytogenetic diagnosis of hereditary diseases associated with diverse anomalies of X chromosome]
Pediatriia 1989;(1):76-80.
1986: Vorsanova S G; Iurov Iu B; Aleksandrov I A; Demidova I A; Mitkevich S P
[Unusual case of 18p- syndrome: diagnosis using a cloned DNA fragment]
T?Sitologii?a i genetika 1986;20(4):291-4.
1986: Vorsanova S G; Yurov Y B; Alexandrov I A; Demidova I A; Mitkevich S P; Tirskaia A F
18p- syndrome: an unusual case and diagnosis by in situ hybridization with chromosome 18-specific alphoid DNA sequence.
Human genetics 1986;72(2):185-7.
1981: Iurov Iu B; Vorsanova S G
[DNA replication in cultured amniotic fluid cells]
Biulleten' eksperimental'noi biologii i meditsiny 1981;92(9):349-52.

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