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المصدر: Human Interphase Chromosomes ISBN: 9783030625313
مصطلحات موضوعية: Molecular cytogenetics, medicine.diagnostic_test, Evolutionary biology, medicine, Fish
, Chromosome, Interphase Chromosome, Genomics, Interphase, Cell cycle, Biology, Fluorescence in situ hybridization URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::3a42e9b497d4babc74b25d4caad005ca
https://doi.org/10.1007/978-3-030-62532-0_7 -
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المؤلفون: Alexei D. Kolotii, I.V. Soloviev, I. A. Demidova, Svetlana G. Vorsanova, Ivan Y. Iourov, Yuri B. Yurov
المصدر: Current Genomics
مصطلحات موضوعية: 0301 basic medicine, Genome instability, Aging, medicine.medical_specialty, Aneuploidy, Human brain, Article, 03 medical and health sciences, Chromosome instability, Gene duplication, Intellectual disability, Genetics, Medicine, Psychiatry, Genetics (clinical), business.industry, Somatic genome variations, Q-FISH, medicine.disease, Chromosomal instability, 030104 developmental biology, Schizophrenia, Ontogeny, Autism, Psychiatric disorders, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c3792a37e80b986daa777b526b65708
https://doi.org/10.2174/1389202918666170717154340 -
3دورية أكاديمية
المؤلفون: Yuri B Yurov, Ivan Y Iourov, Svetlana G Vorsanova, Thomas Liehr, Alexei D Kolotii, Sergei I Kutsev, Franck Pellestor, Alfia K Beresheva, Irina A Demidova, Viktor S Kravets, Viktor V Monakhov, Ilia V Soloviev
المصدر: PLoS ONE, Vol 2, Iss 6, p e558 (2007)
وصف الملف: electronic resource
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المؤلفون: Alexei D. Kolotii, I. V. Kanivets, M. N. Kharabadze, E.A. Nikolaeva, E. Y. Voskoboeva, E. Y. Zakharova, R. G. Kuramagomedova, N. V. Melnikova, Galina Baydakova, A. N. Semyachkina
المصدر: BMC Medical Genetics, Vol 20, Iss 1, Pp 1-8 (2019)
BMC Medical Geneticsمصطلحات موضوعية: 0301 basic medicine, lcsh:Internal medicine, Monosomy, IDS gene, lcsh:QH426-470, Turner syndrome, Mucopolysaccharidosis, Case Report, Iduronate Sulfatase, 030105 genetics & heredity, Biology, Gene mutation, 03 medical and health sciences, Genetics, medicine, Humans, Mucopolysaccharidosis type II, lcsh:RC31-1245, Genetics (clinical), X chromosome, Mucopolysaccharidosis II, Iduronate-2-sulfatase, Мucopolysaccharidosis, Hunter syndrome, medicine.disease, lcsh:Genetics, 030104 developmental biology, Child, Preschool, Female, Iduronate 2-sulfatase
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المؤلفون: Maria A Zelenova, I. A. Demidova, Yuri B. Yurov, Svetlana G. Vorsanova, Alexei D. Kolotii, V.S. Kravets, Ivan Y. Iourov, I.V. Soloviev, Oxana S Kurinnaia
المصدر: OBM Genetics. 3
مصطلحات موضوعية: Epilepsy, Mechanism (biology), Chromosome instability, medicine, Biomarker (medicine), Autism, Aneuploidy, Karyotype, Disease, Biology, medicine.disease, Bioinformatics
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::9613bf0cd7c20c5e3355f308cf5a9def
https://doi.org/10.21926/obm.genet.1901068 -
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المؤلفون: Svetlana G. Vorsanova, V.V. Monakhov, A.K. Beresheva, I. A. Demidova, Alexei D. Kolotii, N. L. Gorbachevskaya, Yuri B. Yurov, Viktoria Y Voinova-Ulas, Ivan Y. Iourov, Viktor S. Kravetz
المصدر: Journal of Medical Genetics. 44:521-525
مصطلحات موضوعية: Male, medicine.medical_specialty, Aneuploidy, Rett syndrome, Biology, Gastroenterology, Neurodevelopmental disorder, Gene Frequency, Internal medicine, Rett Syndrome, Genetics, medicine, Humans, Autistic Disorder, Child, Cells, Cultured, Genetics (clinical), X chromosome, Chromosome Aberrations, Stochastic Processes, Autosome, medicine.diagnostic_test, Mosaicism, Chromosome Mapping, medicine.disease, Developmental disorder, Autism, Letter to JMG, Fluorescence in situ hybridization
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المصدر: Chromosome Research. 14:223-229
مصطلحات موضوعية: Male, medicine.medical_specialty, Aneuploidy, Biology, Molecular cytogenetics, Genetics, medicine, Chromosomes, Human, Humans, Interphase, Metaphase, In Situ Hybridization, Fluorescence, X chromosome, Chromosome Aberrations, Chromosomes, Human, X, Autosome, Mosaicism, Cytogenetics, Chromosome, medicine.disease, Molecular biology, Chromosome Banding, Female, DNA Probes
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المؤلفون: Elena A. Kirillova, Alexei D. Kolotii, V.V. Monakhov, Ivan Y. Iourov, I.V. Soloviev, Svetlana G. Vorsanova, Yuri B. Yurov
المصدر: Journal of Histochemistry & Cytochemistry. 53:375-380
مصطلحات موضوعية: Adult, 0301 basic medicine, Histology, Adolescent, Aneuploidy, In situ hybridization, Biology, Polyploidy, 03 medical and health sciences, medicine, Chromosomes, Human, Humans, Mitosis, In Situ Hybridization, Fluorescence, X chromosome, Chromosome Aberrations, 030102 biochemistry & molecular biology, medicine.diagnostic_test, Mosaicism, Hybridization probe, medicine.disease, Molecular biology, Abortion, Spontaneous, 030104 developmental biology, Chromosome abnormality, Female, Interphase, Anatomy, Fluorescence in situ hybridization
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05c36067f218d23f7874b0bfabf2a25f
https://doi.org/10.1369/jhc.4a6424.2005 -
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المصدر: Molecular Cytogenetics
مصطلحات موضوعية: Senescence, Aging, Pathology, medicine.medical_specialty, Chromosome X, Aneuploidy, Context (language use), Biology, Bioinformatics, Biochemistry, Pathogenesis, Chromosome instability, Genetics, medicine, Genetics(clinical), Molecular Biology, Genetics (clinical), X chromosome, Biochemistry, medical, Molecular cytogenetics, Research, Biochemistry (medical), Cytogenetics, Brain, medicine.disease, Human genetics, Molecular Medicine, Alzheimer’s disease
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المؤلفون: Alexei D. Kolotii, Svetlana G. Vorsanova, Victoria Y. Ulas, A.K. Beresheva, Vasily O. Sharonin, Natalia L. Gorbatchevskaia, I. A. Demidova, Yuri B. Yurov, I.V. Soloviev
المصدر: Brain and Development. 23:S196-S201
مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Pediatrics, Pathology, X Chromosome, Adolescent, Chromosomal Proteins, Non-Histone, Methyl-CpG-Binding Protein 2, DNA Mutational Analysis, Turner Syndrome, Rett syndrome, Biology, Russia, MECP2, Cohort Studies, Klinefelter Syndrome, Neurodevelopmental disorder, Developmental Neuroscience, Dosage Compensation, Genetic, Turner syndrome, Rett Syndrome, medicine, Humans, Genetic Testing, Child, X chromosome, Retrospective Studies, Chromosome Aberrations, medicine.diagnostic_test, Mosaicism, Cytogenetics, Infant, Karyotype, General Medicine, medicine.disease, DNA-Binding Proteins, Repressor Proteins, Child, Preschool, Mutation, Pediatrics, Perinatology and Child Health, Female, Neurology (clinical), Fluorescence in situ hybridization