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Heteromorphic variants of chromosome 9.
Mol Cytogenet. 2013 Apr 1;6(1):14. doi: 10.1186/1755-8166-6-14.
Mol Cytogenet. 2013.
PMID: 23547710
Free PMC article.
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: kulpanovich ai.
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
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Human Ring Chromosomes - New Insights for their Clinical Significance.
Guilherme R, Klein E, Hamid A, Bhatt S, Volleth M, Polityko A, Kulpanovich A, Dufke A, Albrecht B, Morlot S, Brecevic L, Petersen M, Manolakos E, Kosyakova N, Liehr T.
Guilherme R, et al.
Balkan J Med Genet. 2013 Jun;16(1):13-20. doi: 10.2478/bjmg-2013-0013.
Balkan J Med Genet. 2013.
PMID: 24265580
Free PMC article.
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Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres?
Guilherme RS, Klein E, Venner C, Hamid AB, Bhatt S, Melaragno MI, Volleth M, Polityko A, Kulpanovich A, Kosyakova N, Liehr T.
Guilherme RS, et al.
Chromosome Res. 2012 Oct;20(7):825-35. doi: 10.1007/s10577-012-9316-x. Epub 2012 Oct 18.
Chromosome Res. 2012.
PMID: 23076733
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A new multicolor fluorescence in situ hybridization probe set directed against human heterochromatin: HCM-FISH.
Bucksch M, Ziegler M, Kosayakova N, Mulatinho MV, Llerena JC Jr, Morlot S, Fischer W, Polityko AD, Kulpanovich AI, Petersen MB, Belitz B, Trifonov V, Weise A, Liehr T, Hamid AB.
Bucksch M, et al. Among authors: kulpanovich ai.
J Histochem Cytochem. 2012 Jul;60(7):530-6. doi: 10.1369/0022155412441708. Epub 2012 Apr 17.
J Histochem Cytochem. 2012.
PMID: 22511603
Free PMC article.
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Novel data on growth phenotype and causative genotypes in 29 patients with Morquio (Morquio-Brailsford) syndrome from Central-Eastern Europe.
Jezela-Stanek A, Różdżyńska-Świątkowska A, Kulpanovich A, Ciara E, Marucha J, Tylki-Szymańska A.
Jezela-Stanek A, et al.
J Appl Genet. 2019 May;60(2):163-174. doi: 10.1007/s13353-019-00491-1. Epub 2019 Mar 30.
J Appl Genet. 2019.
PMID: 30927141
Free PMC article.
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Mucopolysaccharidosis type VI in Russia, Kazakhstan, and Central and Eastern Europe.
Jurecka A, Zakharova E, Cimbalistiene L, Gusina N, Malinova V, Różdżyńska-Świątkowska A, Golda A, Kulpanovich A, Kaldenovna Abdilova G, Voskoboeva E, Tylki-Szymańska A.
Jurecka A, et al.
Pediatr Int. 2014 Aug;56(4):520-5. doi: 10.1111/ped.12281. Epub 2014 Apr 1.
Pediatr Int. 2014.
PMID: 24373060
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Mucopolysaccharidosis type VI: a predominantly cardiac phenotype associated with homozygosity for p.R152W mutation in the ARSB gene.
Jurecka A, Zakharova E, Cimbalistiene L, Gusina N, Kulpanovich A, Golda A, Opoka-Winiarska V, Piotrowska E, Voskoboeva E, Tylki-Szymańska A.
Jurecka A, et al.
Am J Med Genet A. 2013 Jun;161A(6):1291-9. doi: 10.1002/ajmg.a.35905. Epub 2013 Apr 30.
Am J Med Genet A. 2013.
PMID: 23633437
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