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Year | Number of Results |
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2012 | 1 |
2013 | 2 |
2014 | 1 |
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2024 | 0 |
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Page 1
Somatic mosaicism in the diseased brain.
Mol Cytogenet. 2022 Oct 21;15(1):45. doi: 10.1186/s13039-022-00624-y.
Mol Cytogenet. 2022.
PMID: 36266706
Free PMC article.
Review.
An interstitial deletion at 10q26.2q26.3.
Iourov IY, Vorsanova SG, Kurinnaia OS, Yurov YB.
Iourov IY, et al. Among authors: kurinnaia os.
Case Rep Genet. 2014;2014:505832. doi: 10.1155/2014/505832. Epub 2014 Feb 6.
Case Rep Genet. 2014.
PMID: 24649379
Free PMC article.
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The Cytogenomic "Theory of Everything": Chromohelkosis May Underlie Chromosomal Instability and Mosaicism in Disease and Aging.
Iourov IY, Vorsanova SG, Yurov YB, Zelenova MA, Kurinnaia OS, Vasin KS, Kutsev SI.
Iourov IY, et al. Among authors: kurinnaia os.
Int J Mol Sci. 2020 Nov 6;21(21):8328. doi: 10.3390/ijms21218328.
Int J Mol Sci. 2020.
PMID: 33171981
Free PMC article.
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An interstitial 20q11.21 microdeletion causing mild intellectual disability and facial dysmorphisms.
Iourov IY, Vorsanova SG, Kurinnaia OS, Yurov YB.
Iourov IY, et al. Among authors: kurinnaia os.
Case Rep Genet. 2013;2013:353028. doi: 10.1155/2013/353028. Epub 2013 Feb 14.
Case Rep Genet. 2013.
PMID: 23476833
Free PMC article.
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Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the disease.
Iourov IY, Vorsanova SG, Voinova VY, Kurinnaia OS, Zelenova MA, Demidova IA, Yurov YB.
Iourov IY, et al. Among authors: kurinnaia os.
Mol Cytogenet. 2013 Nov 27;6(1):53. doi: 10.1186/1755-8166-6-53.
Mol Cytogenet. 2013.
PMID: 24283533
Free PMC article.
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Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies.
Iourov IY, Vorsanova SG, Kurinnaia OS, Zelenova MA, Silvanovich AP, Yurov YB.
Iourov IY, et al. Among authors: kurinnaia os.
Mol Cytogenet. 2012 Dec 31;5(1):46. doi: 10.1186/1755-8166-5-46.
Mol Cytogenet. 2012.
PMID: 23272938
Free PMC article.
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