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Cytogenomic epileptology.
Iourov IY, Gerasimov AP, Zelenova MA, Ivanova NE, Kurinnaia OS, Zabrodskaya YM, Demidova IA, Barantsevich ER, Vasin KS, Kolotii AD, Ushanov VV, Sitovskaya DA, Lobzhanidze TB, Iuditskaia ME, Iakushev NS, Zhumatov MM, Vorsanova SG, Samochernyh KA. Iourov IY, et al. Among authors: zelenova ma. Mol Cytogenet. 2023 Jan 5;16(1):1. doi: 10.1186/s13039-022-00634-w. Mol Cytogenet. 2023. PMID: 36600272 Free PMC article. Review.
4q21.2q21.3 Duplication: Molecular and Neuropsychological Aspects.
Iourov IY, Zelenova MA, Vorsanova SG, Voinova VV, Yurov YB. Iourov IY, et al. Among authors: zelenova ma. Curr Genomics. 2018 Apr;19(3):173-178. doi: 10.2174/1389202918666170717161426. Curr Genomics. 2018. PMID: 29606904 Free PMC article. Review.
[Epigenomic variations manifesting as a loss of heterozygosity affecting imprinted genes represent a molecular mechanism of autism spectrum disorders and intellectual disability in children].
Iourov IY, Vorsanova SG, Zelenova MA, Vasin KS, Kurinnaia OS, Korostelev SA, Yurov YB. Iourov IY, et al. Among authors: zelenova ma. Zh Nevrol Psikhiatr Im S S Korsakova. 2019;119(5):91-97. doi: 10.17116/jnevro201911905191. Zh Nevrol Psikhiatr Im S S Korsakova. 2019. PMID: 31317896 Russian.
14 results