Kolotii AD - Search Results

1

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

Vorsanova SG, Demidova IA, Kolotii AD, Kurinnaia OS, Kravets VS, Soloviev IV, Yurov YB, Iourov IY. Vorsanova SG, et al. Among authors: kolotii ad. Mol Cytogenet. 2022 Mar 5;15(1):8. doi: 10.1186/s13039-022-00588-z. Mol Cytogenet. 2022. PMID: 35248137 Free PMC article.

2

[Current methods of molecular cytogenetics in pre- and postnatal diagnosis of chromosome aberrations].

Vorsanova SG, Iurov IuB, Solov'ev IV, Demidova IA, Sharonin VO, Male R, Zhiollant M, Beresheva AK, Kolotiĭ AD, Kravets VS, Ruazes Zh. Vorsanova SG, et al. Among authors: kolotii ad. Klin Lab Diagn. 2000 Aug;(8):36-9. Klin Lab Diagn. 2000. PMID: 11031431 Russian.

3

16q subtelomeric deletion in proband with congenital malformations and mental retardation.

Vorsanova SG, Yurov YB, Kolotii AD, Demidova IA, Novikova IM. Vorsanova SG, et al. Among authors: kolotii ad. Tsitol Genet. 2000 Nov-Dec;34(6):72-4. Tsitol Genet. 2000. PMID: 11394378

4

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

Vorsanova SG, Yurov YB, Kolotii AD, Soloviev IV. Vorsanova SG, et al. Among authors: kolotii ad. Brain Dev. 2001 Dec;23 Suppl 1:S191-5. doi: 10.1016/s0387-7604(01)00364-3. Brain Dev. 2001. PMID: 11738871

5

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).

Vorsanova SG, Yurov YB, Ulas VY, Demidova IA, Sharonin VO, Kolotii AD, Gorbatchevskaia NL, Beresheva AK, Soloviev IV. Vorsanova SG, et al. Among authors: kolotii ad. Brain Dev. 2001 Dec;23 Suppl 1:S196-201. doi: 10.1016/s0387-7604(01)00347-3. Brain Dev. 2001. PMID: 11738872

6

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

Yurov YB, Vorsanova SG, Kolotii AD, Iourov IY. Yurov YB, et al. Among authors: kolotii ad. Brain Dev. 2001 Dec;23 Suppl 1:S214-7. doi: 10.1016/s0387-7604(01)00370-9. Brain Dev. 2001. PMID: 11738875

7

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

Iourov IY, Liehr T, Vorsanova SG, Kolotii AD, Yurov YB. Iourov IY, et al. Among authors: kolotii ad. Chromosome Res. 2006;14(3):223-9. doi: 10.1007/s10577-006-1037-6. Epub 2006 Apr 20. Chromosome Res. 2006. PMID: 16628493

8

Pericentric inversion inv(7)(p11q21.1): report on two cases and genotype-phenotype correlations.

Vorsanova SG, Iourov IY, Demidova IA, Kolotii AD, Soloviev IV, Yurov YB. Vorsanova SG, et al. Among authors: kolotii ad. Tsitol Genet. 2006 May-Jun;40(3):45-8. Tsitol Genet. 2006. PMID: 16933852

9

Unexplained autism is frequently associated with low-level mosaic aneuploidy.

Yurov YB, Vorsanova SG, Iourov IY, Demidova IA, Beresheva AK, Kravetz VS, Monakhov VV, Kolotii AD, Voinova-Ulas VY, Gorbachevskaya NL. Yurov YB, et al. Among authors: kolotii ad. J Med Genet. 2007 Aug;44(8):521-5. doi: 10.1136/jmg.2007.049312. Epub 2007 May 4. J Med Genet. 2007. PMID: 17483303 Free PMC article.

10

[Chromosomal mosaicism in spontaneous abortions: analysis of 650 cases].

Vorsanova SG, Iurov IIu, Kolotiĭ AD, Beresheva AK, Demidova IA, Kurinnaia OS, Kravets VS, Monakhov VV, Solov'ev IV, Iurov IuB. Vorsanova SG, et al. Among authors: kolotii ad. Genetika. 2010 Oct;46(10):1356-9. Genetika. 2010. PMID: 21254555 Russian.

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