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Please use this identifier to cite or link to this item: http://dspace.bsu.edu.ru/handle/123456789/41334
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dc.contributor.authorVorsanova, S. G.-
dc.contributor.authorKolotii, A. D.-
dc.contributor.authorKurinnaia, O. S.-
dc.contributor.authorKravets, V. S.-
dc.contributor.authorIourov, I. Y-
dc.date.accessioned2021-06-07T07:49:54Z-
dc.date.available2021-06-07T07:49:54Z-
dc.date.issued2021-
dc.identifier.citationTurner’s syndrome mosaicism in girls with neurodevelopmental disorders: a cohort study and hypothesis / S.G. Vorsanova [et al.] // Molecular Cytogenetics. - 2021. - Vol.14.-Art. 9. - Doi: https://doi.org/10.1186/s13039-021-00529-2. - URL: https://molecularcytogenetics.biomedcentral.com/articles/10.1186/s13039-021-00529-2ru
dc.identifier.urihttp://dspace.bsu.edu.ru/handle/123456789/41334-
dc.description.abstractTurner’s syndrome is associated with either monosomy or a wide spectrum of structural rearrangements of chromosome X. Despite the interest in studying (somatic) chromosomal mosaicism, Turner’s syndrome mosaicism (TSM) remains to be fully described. This is especially true for the analysis of TSM in clinical cohorts (e.g. cohorts of individuals with neurodevelopmental disorders). Here, we present the results of studying TSM in a large cohort of girls with neurodevelopmental disorders and a hypothesis highlighting the diagnostic and prognostic valueru
dc.language.isoenru
dc.subjectbiologyru
dc.subjectgeneticsru
dc.subjectaneuploidyru
dc.subjectchromosome Xru
dc.subjectfluorescence in situ hybridization (FISH)ru
dc.subjectmolecular cytogeneticsru
dc.subjectphenotyperu
dc.subjectsomatic mosaicismru
dc.subjectTurner’s syndromeru
dc.titleTurner’s syndrome mosaicism in girls with neurodevelopmental disorders: a cohort study and hypothesisru
dc.typeArticleru
Appears in Collections:Статьи из периодических изданий и сборников (на иностранных языках) = Articles from periodicals and collections (in foreign languages)

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