S. Vorsanova

发表

Y. Yurov, S. Vorsanova, I. Iourov, 2013, Springer New York.

An Approach for Quantitative Assessment of Fluorescence In Situ Hybridization (FISH) Signals for Applied Human Molecular Cytogenetics

I. V. Soloviev, Y. Yurov, S. Vorsanova, 2005, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Detection of Circulating Serum microRNA/Protein Complexes in ASD Using Functionalized Chips for an Atomic Force Microscope

A. A. Valueva, I. D. Shumov, A. Archakov, 2021, Molecules.

The Cytogenomic “Theory of Everything”: Chromohelkosis May Underlie Chromosomal Instability and Mosaicism in Disease and Aging

Y. Yurov, S. Vorsanova, I. Iourov, 2020, International journal of molecular sciences.

Turner’s syndrome mosaicism in girls with neurodevelopmental disorders: a cohort study and hypothesis

Y. Yurov, S. Vorsanova, I. Iourov, 2021, Molecular cytogenetics.

The variome concept: focus on CNVariome

Y. Yurov, S. Vorsanova, I. Iourov, 2019, Molecular Cytogenetics.

Pathway-based classification of genetic diseases

Y. Yurov, S. Vorsanova, I. Iourov, 2019, Molecular Cytogenetics.

In silico molecular cytogenetics: a bioinformatic approach to prioritization of candidate genes and copy number variations for basic and clinical genome research

Y. Yurov, S. Vorsanova, I. Iourov, 2014, Molecular Cytogenetics.

Cytogenomic landscape of the human brain

Y. Yurov, S. Vorsanova, I. Iourov, 2021 .

Multicolor fluorescent in situ hybridization on post-mortem brain in schizophrenia as an approach for identification of low-level chromosomal aneuploidy in neuropsychiatric diseases

Y. Yurov, S. Vorsanova, I. Iourov, 2001, Brain and Development.

Chromosomal mosaicism in spontaneous abortions: Analysis of 650 cases

I. V. Soloviev, Y. Yurov, S. Vorsanova, 2010, Russian Journal of Genetics.

COVID-19 and Aging-Related Genome (Chromosome) Instability in the Brain: Another Possible Time-Bomb of SARS-CoV-2 Infection

S. Vorsanova, I. Iourov, 2022, Frontiers in Aging Neuroscience.

Long contiguous stretches of homozygosity spanning shortly the imprinted loci are associated with intellectual disability, autism and/or epilepsy

Y. Yurov, S. Vorsanova, I. Iourov, 2015, Molecular Cytogenetics.

Pilot data of serum proteins from children with autism spectrum disorders

Y. Ivanov, S. Vorsanova, I. Iourov, 2019, Data in brief.

The Cytogenomic “Theory of Everything”: Chromohelkosis May Underlie Chromosomal Instability and Mosaicism in Disease and Aging

Y. Yurov, S. Vorsanova, I. Iourov, 2020, International journal of molecular sciences.

FISH analysis of replication and transcription of chromosome X loci: new approach for genetic analysis of Rett syndrome

I. V. Soloviev, Y. Yurov, S. Vorsanova, 2001, Brain and Development.

Serologic Markers of Autism Spectrum Disorder

Y. Ivanov, A. Archakov, Y. Yurov, 2017, Journal of Molecular Neuroscience.

Proteomic analysis of serum proteins of children with autism

A. Archakov, Y. Ivanov, Y. Yurov, 2017 .

Proteomic analysis of blood serum protein profiles in children with autism

A. Archakov, Y. Ivanov, S. Vorsanova, 2016 .

[Clinical and genetic characteristics of the X chromosome distal long arm microduplications encompassing the MECP2 gene].

Y. Yurov, S. Vorsanova, I. Iourov, 2015, Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova.

Klinefelter syndrome mosaicism in boys with neurodevelopmental disorders: a cohort study and an extension of the hypothesis

Y. Yurov, S. Vorsanova, I. Iourov, 2022, Molecular cytogenetics.

Evidence for High Frequency of Chromosomal Mosaicism in Spontaneous Abortions Revealed by Interphase FISH Analysis

I. V. Soloviev, Y. Yurov, S. Vorsanova, 2005, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

CHROMOHELKOSIS — A UNUSUAL FORM OF CHROMOSOME INSTABILITY AND SOMATIC MOSAICISM ASSOCIATED WITH CENTRAL NERVOUS SYSTEM DISEASES IN CHILDREN

Y. Yurov, S. Vorsanova, I. Iourov, 2021, Современные проблемы науки и образования (Modern Problems of Science and Education).

Rett syndrome in Russia and abroad: a scientific historical review

S. Vorsanova, V. Voinova, I. Yurov, 2020, Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics).

VIII World Rett Syndrome Congress & Symposium of rare diseases, Kazan, Russia

Y. Yurov, S. Vorsanova, I. Iourov, 2018, Molecular Cytogenetics.

An Interstitial 20q11.21 Microdeletion Causing Mild Intellectual Disability and Facial Dysmorphisms

Y. Yurov, S. Vorsanova, I. Iourov, 2013, Case reports in genetics.

Somatic mosaicism in the diseased brain

Y. Yurov, S. Vorsanova, I. Iourov, 2022, Molecular Cytogenetics.

4q21.2q21.3 Duplication: Molecular and Neuropsychological Aspects

Y. Yurov, S. Vorsanova, I. Iourov, 2017, Current genomics.

Chromosome Instability in the Neurodegenerating Brain

Y. Yurov, S. Vorsanova, I. Iourov, 2019, Front. Genet..

Current Pharmaceutical Biotechnology

Y. Yurov, S. Vorsanova, I. Iourov, 2021 .

The applicability of interphase chromosome-specific multicolor banding (ICS-MCB) for studying neurodevelopmental and neurodegenerative disorders

T. Liehr, Y. Yurov, S. Vorsanova, 2019, Research Results in Biomedicine.

Human Molecular Neurocytogenetics

Y. Yurov, S. Vorsanova, I. Iourov, 2018, Current Genetic Medicine Reports.

Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies

Y. Yurov, S. Vorsanova, I. Iourov, 2012, Molecular Cytogenetics.

Identification of candidate genes of autism on the basis of molecular cytogenetic and in silico studies of the genome organization of chromosomal regions involved in unbalanced rearrangements

Y. Yurov, S. Vorsanova, I. Iourov, 2010, Russian Journal of Genetics.

Interphase Chromosomes of the Human Brain

Y. Yurov, S. Vorsanova, I. Iourov, 2020 .

Culture method for amniotic fluid cells

S. Vorsanova, 1979, Bulletin of Experimental Biology and Medicine.

Cytogenomic epileptology

S. Vorsanova, I. Iourov, I. Demidova, 2023, Molecular Cytogenetics.

Ontogenetic Variation of the Human Genome

Y. Yurov, S. Vorsanova, I. Iourov, 2010, Current genomics.

Human interphase chromosomes: a review of available molecular cytogenetic technologies

Y. Yurov, S. Vorsanova, I. Iourov, 2010, Molecular Cytogenetics.

Recent patents on molecular cytogenetics.

Y. Yurov, S. Vorsanova, I. Iourov, 2008, Recent Patents on DNA & Gene Sequences.

Characteristics of human embryonic hepatocytes cultivated in vitro

S. Vorsanova, T. L. Éraizer, K. Grinberg, 1975, Bulletin of Experimental Biology and Medicine.

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

I. V. Soloviev, Y. Yurov, S. Vorsanova, 1996, Molecular human reproduction.

Twenty-First Century FISH: Focus on Interphase Chromosomes

Y. Yurov, S. Vorsanova, I. Iourov, 2020 .

Ontogenetic and Pathogenetic Views on Somatic Chromosomal Mosaicism

Y. Yurov, S. Vorsanova, I. Iourov, 2019, Genes.

Yuri B. Yurov (1951-2017)

S. Vorsanova, I. Iourov, 2018, Molecular Cytogenetics.

FISH-Based Assays for Detecting Genomic (Chromosomal) Mosaicism in Human Brain Cells

I. V. Soloviev, Y. Yurov, S. Vorsanova, 2017 .

Interphase FISH for Detection of Chromosomal Mosaicism

Y. Yurov, S. Vorsanova, I. Iourov, 2017 .

Long contiguous stretches of homozygosity spanning shortly the imprinted loci are associated with intellectual disability, autism and/or epilepsy

Y. Yurov, S. Vorsanova, I. Iourov, 2015, Molecular Cytogenetics.

In silico molecular cytogenetics: a bioinformatic approach to prioritization of candidate genes and copy number variations for basic and clinical genome research

Y. Yurov, S. Vorsanova, I. Iourov, 2014, Molecular Cytogenetics.

Technological Solutions in Human Interphase Cytogenetics

Y. Yurov, S. Vorsanova, I. Iourov, 2013 .

Introduction to Interphase Molecular Cytogenetics

Y. Yurov, S. Vorsanova, I. Iourov, 2013 .

Single Cell Genomics of the Brain: Focus on Neuronal Diversity and Neuropsychiatric Diseases

Y. Yurov, S. Vorsanova, I. Iourov, 2012, Current genomics.

Molecular Cytogenetic Diagnosis and Somatic Genome Variations

Y. Yurov, S. Vorsanova, I. Iourov, 2010, Current genomics.

Molecular Cytogenetics and Cytogenomics of Brain Diseases

Y. Yurov, S. Vorsanova, I. Iourov, 2008, Current genomics.

Detection of Aneuploidy in Neural Stem Cells of the Developingand Adult Human Brain

Y. Yurov, S. Vorsanova, I. Iourov, 2008 .

Human Interphase Cytogenomics

Y. Yurov, S. Vorsanova, I. Iourov, 2020 .

Chromosomal variation in mammalian neuronal cells: known facts and attractive hypotheses.

Y. Yurov, S. Vorsanova, I. Iourov, 2006, International review of cytology.

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

Y. Yurov, S. Vorsanova, A. Laurent, 1995, Human Genetics.

Opening up new horizons for psychiatric genetics in the Russian Federation: moving toward a national consortium

T. Schulze, R. Gainetdinov, E. Khusnutdinova, 2019, Molecular Psychiatry.

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

I. V. Soloviev, Y. Yurov, S. Vorsanova, 1995, Prenatal diagnosis.

X chromosome aneuploidy in the Alzheimer’s disease brain

T. Liehr, Y. Yurov, S. Vorsanova, 2014, Molecular Cytogenetics.

Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia

T. Liehr, Y. Yurov, S. Vorsanova, 2008, Cytogenetic and Genome Research.

Chromosome Instability, Aging and Brain Diseases

Y. Yurov, S. Vorsanova, I. Iourov, 2021, Cells.

The variome concept: focus on CNVariome

Y. Yurov, S. Vorsanova, I. Iourov, 2019, Molecular cytogenetics.

Chromosomal mosaicism goes global

Y. Yurov, S. Vorsanova, I. Iourov, 2008, Molecular Cytogenetics.

3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances

Y. Yurov, S. Vorsanova, I. Iourov, 2015, Molecular Cytogenetics.

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

I. V. Soloviev, T. Liehr, Y. Yurov, 2008, Molecular Cytogenetics.

5p13.3p13.2 duplication associated with developmental delay, congenital malformations and chromosome instability manifested as low-level aneuploidy

Y. Yurov, S. Vorsanova, I. Iourov, 2015, SpringerPlus.

Genomic Copy Number Variation Affecting Genes Involved in the Cell Cycle Pathway: Implications for Somatic Mosaicism

Y. Yurov, S. Vorsanova, I. Iourov, 2015, International journal of genomics.

DNA replication in amniotic fluid cells in culture

Y. Yurov, S. Vorsanova, 1981, Bulletin of Experimental Biology and Medicine.

Heteromorphic variants of chromosome 9

S. Bhatt, T. Liehr, R. Wegner, 2013, Molecular Cytogenetics.

Instability of chromosomes in human nerve cells (Normal and with Neuromental Diseases)

Y. Yurov, S. Vorsanova, I. Iourov, 2010, Russian Journal of Genetics.

Cytogenetic, Molecular-Cytogenetic, and Clinical-Genealogical Studies of the Mothers of Children with Autism: A Search for Familial Genetic Markers for Autistic Disorders

Y. Yurov, S. Vorsanova, I. Demidova, 2010, Neuroscience and Behavioral Physiology.

Cytogenetic analysis in the era of highresolution molecular-cytogenetic methods: the potential of «reverse» karyotyping

Y. Yurov, S. Vorsanova, I. Iourov, 2019, Research Results in Biomedicine.

Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the disease

Y. Yurov, S. Vorsanova, I. Iourov, 2013, Molecular Cytogenetics.

Somatic Genome Variations in Health and Disease

Y. Yurov, S. Vorsanova, I. Iourov, 2010, Current genomics.

A new open access journal for a rapidly evolving biomedical field: introducing Molecular Cytogenetics

L. Shaffer, T. Liehr, Y. Yurov, 2008, Molecular Cytogenetics.

Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the disease

Y. Yurov, S. Vorsanova, I. Iourov, 2013, Molecular Cytogenetics.

Interphase chromosome-specific multicolor banding (ICS-MCB): a new tool for analysis of interphase chromosomes in their integrity.

T. Liehr, Y. Yurov, S. Vorsanova, 2007, Biomolecular engineering.

Somatic Cell Genomics of Brain Disorders: A New Opportunity to Clarify Genetic-Environmental Interactions

Y. Yurov, S. Vorsanova, I. Iourov, 2013, Cytogenetic and Genome Research.

Investigation of stationary populations of genetically different homonuclear strains of human cells

S. Vorsanova, 1978, Bulletin of Experimental Biology and Medicine.

Pathway-based classification of genetic diseases

Y. Yurov, S. Vorsanova, I. Iourov, 2019, Molecular Cytogenetics.

Aneuploidy in the normal, Alzheimer's disease and ataxia-telangiectasia brain: Differential expression and pathological meaning

T. Liehr, Y. Yurov, S. Vorsanova, 2009, Neurobiology of Disease.

Aneuploidy and Confined Chromosomal Mosaicism in the Developing Human Brain

I. V. Soloviev, T. Liehr, Y. Yurov, 2007, PloS one.

Visualization of interphase chromosomes in postmitotic cells of the human brain by multicolour banding (MCB)

T. Liehr, Y. Yurov, S. Vorsanova, 2006, Chromosome Research.

Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain.

T. Liehr, Y. Yurov, S. Vorsanova, 2009, Human molecular genetics.

Neurological, genetic and epigenetic features of Rett syndrome

Y. Yurov, S. Vorsanova, I. Iourov, 2004, Journal of Pediatric Neurology.

Chromosome-Centric Look at the Genome

Y. Yurov, S. Vorsanova, I. Iourov, 2020 .

Methods of molecular cytogenetics for studying interphase chromosomes in human brain cells

Y. Yurov, S. Vorsanova, I. Iourov, 2010, Russian Journal of Genetics.

Fluorescence intensity profiles of in situ hybridization signals depict genome architecture within human interphase nuclei

Y. Yurov, S. Vorsanova, I. Iourov, 2008, Cytology and Genetics.

Interphase Chromosomes of the Human Brain: The Biological and Clinical Meaning of Neural Aneuploidy

Y. Yurov, S. Vorsanova, I. Iourov, 2013 .

Heteromorphic variants of chromosome 9

S. Bhatt, T. Liehr, R. Wegner, 2013, Molecular Cytogenetics.

The schizophrenia brain exhibits low-level aneuploidy involving chromosome 1

I. V. Soloviev, T. Liehr, Y. Yurov, 2008, Schizophrenia Research.

Systems Cytogenomics: Are We Ready Yet?

Y. Yurov, S. Vorsanova, I. Iourov, 2021, Current genomics.

X chromosome aneuploidy in the Alzheimer’s disease brain

T. Liehr, Y. Yurov, S. Vorsanova, 2014, Molecular Cytogenetics.

Systems Biology Analysis and Literature Data Mining for Unmasking Pathogenic Neurogenomic Variations in Clinical Molecular Diagnosis

Ivan Y. Iourov, Svetlana G. Vorsanova, Yuri B. Yurov, 2018, BIOINFORMATICS.

The Variation of Aneuploidy Frequency in the Developing and Adult Human Brain Revealed by an Interphase FISH Study

I. V. Soloviev, Y. Yurov, S. Vorsanova, 2005, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

“Silicon-On-Insulator”-Based Nanosensor for the Revelation of MicroRNA Markers of Autism

I. D. Shumov, A. Archakov, Y. Ivanov, 2022, Genes.

An Interstitial Deletion at 10q26.2q26.3

Y. Yurov, S. Vorsanova, I. Iourov, 2014, Case reports in genetics.

Laundering CNV data for candidate process prioritization in brain disorders

Y. Yurov, S. Vorsanova, I. Iourov, 2019, Molecular Cytogenetics.

The DNA Replication Stress Hypothesis of Alzheimer's Disease

Y. Yurov, S. Vorsanova, I. Iourov, 2012, TheScientificWorldJournal.

Genomic Landscape of the Alzheimer’s Disease Brain: Chromosome Instability – Aneuploidy, but Not Tetraploidy – Mediates Neurodegeneration

Y. Yurov, S. Vorsanova, I. Iourov, 2010, Neurodegenerative Diseases.

Molecular-cytogenetic investigation of skewed chromosome X inactivation in Rett syndrome

Y. Yurov, S. Vorsanova, I. Iourov, 2001, Brain and Development.

Cytogenetic and molecular‐cytogenetic investigation of Rett syndrome: analysis of 31 cases

V. Y. Ulas, Y. Yurov, S. Vorsanova, 1996, Neuroreport.

Neurodegeneration mediated by chromosome instability suggests changes in strategy for therapy development in ataxia-telangiectasia.

Y. Yurov, S. Vorsanova, I. Iourov, 2009, Medical hypotheses.

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)

I. V. Soloviev, V. Y. Ulas, Y. Yurov, 2001, Brain and Development.

FISHing for Unstable Cellular Genomes in the Human Brain

Y. Yurov, S. Vorsanova, I. Iourov, 2019, OBM Genetics.

Mosaic Brain Aneuploidy in Mental Illnesses: An Association of Low-level Post-zygotic Aneuploidy with Schizophrenia and Comorbid Psychiatric Disorders

I. V. Soloviev, Y. Yurov, S. Vorsanova, 2017, Current genomics.

Dynamic nature of somatic chromosomal mosaicism, genetic-environmental interactions and therapeutic opportunities in disease and aging

Y. Yurov, S. Vorsanova, I. Iourov, 2020, Molecular Cytogenetics.

40-Hz Auditory Steady-State Response (ASSR) as a Biomarker of Genetic Defects in the SHANK3 Gene: A Case Report of 15-Year-Old Girl with a Rare Partial SHANK3 Duplication

G. Portnova, S. Vorsanova, I. Iourov, 2021, International journal of molecular sciences.

Unexplained autism is frequently associated with low-level mosaic aneuploidy

Y. Yurov, S. Vorsanova, I. Demidova, 2007, Journal of Medical Genetics.

Developmental neural chromosome instability as a possible cause of childhood brain cancers.

Y. Yurov, S. Vorsanova, I. Iourov, 2009, Medical hypotheses.

Clinical, neurophysiological and immunological correlations in classical Rett syndrome

Vitali V. Gratchev, S. Vorsanova, V. Bashina, 2001, Brain and Development.

VIII World Rett Syndrome Congress & Symposium of rare diseases, Kazan, Russia

Y. Yurov, S. Vorsanova, I. Iourov, 2018, Molecular Cytogenetics.

Dynamic nature of somatic chromosomal mosaicism, genetic-environmental interactions and therapeutic opportunities in disease and aging

Y. Yurov, S. Vorsanova, I. Iourov, 2020, Molecular Cytogenetics.

Laundering CNV data for candidate process prioritization in brain disorders

Y. Yurov, S. Vorsanova, I. Iourov, 2019, Molecular Cytogenetics.

BIOMARKERS FOR CHILDHOOD NONMALIGNANT BRAIN DISEASES ASSOCAITED WITH CHROMOSOME INSTABILITY

Y. Yurov, S. Vorsanova, I. Iourov, 2018, Research Result Medicine and Pharmacy.

Behavioral Variability and Somatic Mosaicism: A Cytogenomic Hypothesis

Y. Yurov, S. Vorsanova, I. Iourov, 2017, Current genomics.

Ataxia-telangiectasia paradoxes: spotlight on post-zygotic chromosome instability in the brain and its contribution to neurodegeneration pathways

T. Liehr, Y. Yurov, S. Vorsanova, 2013, Molecular Neurodegeneration.

Somatic Genome Variations

Y. Yurov, S. Vorsanova, I. Iourov, 2012 .

GIN'n'CIN hypothesis of brain aging: deciphering the role of somatic genetic instabilities and neural aneuploidy during ontogeny

Y. Yurov, S. Vorsanova, I. Iourov, 2009, Molecular Cytogenetics.

[Genomic instability in the brain: chromosomal mosaicism in schizophrenia].

N. Uranova, Y. Yurov, S. Vorsanova, 2016, Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova.

Interphase Chromosome-Specific Multicolor Banding

T. Liehr, Y. Yurov, S. Vorsanova, 2013 .

Genetic Mechanisms of Mental Disturbances: Chromosomal and Genomic Disorders

S. Vorsanova, Yurov I.Yu., Yurov Yu.B., 2010 .

Intercellular Genomic (Chromosomal) Variations Resulting in Somatic Mosaicism: Mechanisms and Consequences

Y. Yurov, S. Vorsanova, I. Iourov, 2006 .

Ataxia telangiectasia paradox can be explained by chromosome instability at the subtissue level.

Y. Yurov, S. Vorsanova, I. Iourov, 2007, Medical hypotheses.

Brain tissue preparations for chromosomal PRINS labeling.

Y. Yurov, S. Vorsanova, I. Iourov, 2006, Methods in molecular biology.

Maternal smoking as a cause of mosaic aneuploidy in spontaneous abortions.

Y. Yurov, S. Vorsanova, I. Iourov, 2008, Medical hypotheses.

First case of del(1)(p36.2p33) in a fetus delivered stillborn

Y. Yurov, S. Vorsanova, I. Iourov, 2006, Prenatal diagnosis.

HUMAN EMBRYONIC PREALBUMIN AS A MARKER FOR TUMOURS AND FIBROBLASTS

V. Kalashnikov, S. Vorsanova, M. Vasiliev, 1978, The Lancet.

[Structural variations of the genome in autistic spectrum disorders with intellectual disability].

Y. Yurov, S. Vorsanova, I. Iourov, 2016, Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova.

Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain.

T. Liehr, Y. Yurov, S. Vorsanova, 2009, Human molecular genetics.

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

Y. Yurov, S. Vorsanova, S. P. Mitkevich, 1986, Human genetics.

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

I. V. Soloviev, Y. Yurov, S. Vorsanova, 1996, Human Genetics.