Rumyantseva NV - Search Results

1

Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome.

Polityko AD, Khurs OM, Kulpanovich AI, Mosse KA, Solntsava AV, Rumyantseva NV, Naumchik IV, Liehr T, Weise A, Mkrtchyan H. Polityko AD, et al. Among authors: rumyantseva nv. Eur J Med Genet. 2009 Jul-Aug;52(4):207-10. doi: 10.1016/j.ejmg.2009.03.016. Epub 2009 Apr 16. Eur J Med Genet. 2009. PMID: 19375526

2

Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype.

Vermeesch JR, Melotte C, Salden I, Riegel M, Trifnov V, Polityko A, Rumyantseva N, Naumchik I, Starke H, Matthijs G, Schinzel A, Fryns JP, Liehr T. Vermeesch JR, et al. Eur J Med Genet. 2005 Jul-Sep;48(3):319-27. doi: 10.1016/j.ejmg.2005.04.018. Eur J Med Genet. 2005. PMID: 16179227

3

Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding.

Polityko A, Starke H, Rumyantseva N, Claussen U, Liehr T, Raskin S. Polityko A, et al. Cytogenet Genome Res. 2005;111(2):171-4. doi: 10.1159/000086388. Cytogenet Genome Res. 2005. PMID: 16103660

4

Two further AHO-like syndrome patients with deletion of glypican 1 gene region in 2q37.2-q37.3.

Polityko A, Maltseva O, Rumyantseva N, Khurs O, Seidel J, Claussen U, Weise A, Liehr T, Starke H. Polityko A, et al. Int J Mol Med. 2004 Dec;14(6):977-9. Int J Mol Med. 2004. PMID: 15547662

5

Pallister-Killian syndrome: rapid decrease of isochromosome 12p frequency during amniocyte subculturing. Conclusion for strategy of prenatal cytogenetic diagnostics.

Polityko AD, Goncharova E, Shamgina L, Drozdovskaja N, Podleschuk L, Abramchik E, Jaroshevich E, Khurs O, Pisarik I, Pribushenya O, Rumyantseva N, Naumchik I. Polityko AD, et al. J Histochem Cytochem. 2005 Mar;53(3):361-4. doi: 10.1369/jhc.4A6402.2005. J Histochem Cytochem. 2005. PMID: 15750020

6

Trisomy 2p: analysis of unusual phenotypic findings.

Lurie IW, Ilyina HG, Gurevich DB, Rumyantseva NV, Naumchik IV, Castellan C, Hoeller A, Schinzel A. Lurie IW, et al. Among authors: rumyantseva nv. Am J Med Genet. 1995 Jan 16;55(2):229-36. doi: 10.1002/ajmg.1320550216. Am J Med Genet. 1995. PMID: 7717424 Review.

7

Further delineation of the branchio-oculo-facial syndrome.

Lin AE, Gorlin RJ, Lurie IW, Brunner HG, van der Burgt I, Naumchik IV, Rumyantseva NV, Stengel-Rutkowski S, Rosenbaum K, Meinecke P, et al. Lin AE, et al. Among authors: rumyantseva nv. Am J Med Genet. 1995 Mar 13;56(1):42-59. doi: 10.1002/ajmg.1320560112. Am J Med Genet. 1995. PMID: 7747785 Free article. Review.

8

Two siblings with immunodeficiency, facial abnormalities and chromosomal instability without mutation in DNMT3B gene but liability towards malignancy; a new chromatin disorder delineation?

Polityko A, Khurs O, Rumyantseva N, Naumchik I, Kosyakova N, Tönnies H, Sperling K, Neitzel H, Weise A, Liehr T. Polityko A, et al. Mol Cytogenet. 2010 Mar 8;3:5. doi: 10.1186/1755-8166-3-5. Mol Cytogenet. 2010. PMID: 20211012 Free PMC article.

9

Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect.

Barber JC, Zhang S, Friend N, Collins AL, Maloney VK, Hastings R, Farren B, Barnicoat A, Polityko AD, Rumyantseva NV, Starke H, Ye S. Barber JC, et al. Among authors: rumyantseva nv. Cytogenet Genome Res. 2006;114(3-4):351-8. doi: 10.1159/000094225. Cytogenet Genome Res. 2006. PMID: 16954678

10

Trisomy 20p: case report and genetic review.

Lurie IW, Rumyantseva NV, Zaletajev DV, Gurevich DB, Korotkova IA. Lurie IW, et al. Among authors: rumyantseva nv. J Genet Hum. 1985 Jan;33(1):67-75. J Genet Hum. 1985. PMID: 3981145

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