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Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization.
Manolakos E, Kefalas K, Neroutsou R, Lagou M, Kosyakova N, Ewers E, Ziegler M, Weise A, Tsoplou P, Rapti SM, Papoulidis I, Anastasakis E, Garas A, Sotiriou S, Eleftheriades M, Peitsidis P, Malathrakis D, Thomaidis L, Kitsos G, Orru S, Liehr T, Petersen MB, Kitsiou-Tzeli S. Manolakos E, et al. Among authors: ewers e. Mol Med Rep. 2010 Nov-Dec;3(6):1015-22. doi: 10.3892/mmr.2010.358. Epub 2010 Sep 10. Mol Med Rep. 2010. PMID: 21472348
New cytogenetically visible copy number variant in region 8q21.2.
Manvelyan M, Cremer FW, Lancé J, Kläs R, Kelbova C, Ramel C, Reichenbach H, Schmidt C, Ewers E, Kreskowski K, Ziegler M, Kosyakova N, Liehr T. Manvelyan M, et al. Among authors: ewers e. Mol Cytogenet. 2011 Jan 5;4(1):1. doi: 10.1186/1755-8166-4-1. Mol Cytogenet. 2011. PMID: 21208402 Free PMC article.
Small supernumerary marker chromosomes 1 with a normal phenotype.
Liehr T, Wegner RD, Stumm M, Martin T, Gillessen-Kaesbach G, Kosyakova N, Ewers E, Hamid AB, von Eggeling F, Hentschel J, Ziegler M, Weise A. Liehr T, et al. Among authors: ewers e. J Chin Med Assoc. 2010 Apr;73(4):205-7. doi: 10.1016/S1726-4901(10)70042-3. J Chin Med Assoc. 2010. PMID: 20457442 Free article.
68 results