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Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four-break rearrangement.
Manolakos E, Vetro A, Papadopoulou E, Kefalas K, Lagou M, Thomaidis L, Peitsidis P, Sifakis S, Divane A, Ziegler M, Liehr T, Zuffardi O, Papoulidis I. Manolakos E, et al. Among authors: kefalas k. Cytogenet Genome Res. 2013;140(1):12-20. doi: 10.1159/000350868. Epub 2013 May 4. Cytogenet Genome Res. 2013. PMID: 23652918
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: kefalas k. 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
Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature.
Manolakos E, Vetro A, Garas A, Thomaidis L, Kefalas K, Kitsos G, Ziegler M, Liehr T, Zuffardi O, Papoulidis I. Manolakos E, et al. Among authors: kefalas k. Exp Ther Med. 2014 Apr;7(4):953-957. doi: 10.3892/etm.2014.1520. Epub 2014 Feb 6. Exp Ther Med. 2014. PMID: 24669257 Free PMC article.
Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH.
Manolakos E, Kefalas K, Vetro A, Oikonomidou E, Daskalakis G, Psara N, Siomou E, Papageorgiou E, Sevastopoulou E, Konstantinidou A, Vrachnis N, Thomaidis L, Zuffardi O, Papoulidis I. Manolakos E, et al. Among authors: kefalas k. Mol Cytogenet. 2013 Oct 31;6(1):47. doi: 10.1186/1755-8166-6-47. Mol Cytogenet. 2013. PMID: 24176130 Free PMC article.
Deletion 2q31.2-q31.3 in a 4-year-old girl with microcephaly and severe mental retardation.
Manolakos E, Vetro A, Kefalas K, Thomaidis L, Aperis G, Sotiriou S, Kitsos G, Merkas M, Sifakis S, Papoulidis I, Liehr T, Zuffardi O, Petersen MB. Manolakos E, et al. Among authors: kefalas k. Am J Med Genet A. 2011 Jun;155A(6):1476-82. doi: 10.1002/ajmg.a.33981. Epub 2011 May 12. Am J Med Genet A. 2011. PMID: 21567918 No abstract available.
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