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Placenta|November 25, 2010
Non-trophoblastic tumor of the placenta with combined histologic features of chorangioma and leiomyomaD Miliaras, E Anagnostou, I Papoulidis, et al.Journal of Medical Case Reports|November 3, 2019
Lowe syndrome identified in the offspring of an oocyte donor who was an unknown carrier of a de novo mutation: a case report and review of the literatureP Tatsi, G E Papanikolaou, T Chartomatsidou, et al.Clinical and Experimental Obstetrics & Gynecology|June 9, 2012
First trimester diagnosis of 13q-syndrome associated with increased fetal nuchal translucency thickness. Clinical findings and systematic reviewE Manolakos, P Peitsidis, A Garas, et al.Molecular Syndromology|July 26, 2013
De novo 15.5-Mb Interstitial Deletion in 5p in a Male Ascertained by OligospermiaI Papoulidis, A Vetro, K Kefalas, et al.Gene|December 17, 2013
A patient with partial trisomy 21 and 7q deletion expresses mild Down syndrome phenotypeI Papoulidis, E Papageorgiou, E Siomou, et al.Molecular Cytogenetics|August 4, 2016
Partial monosomy14q involving FOXG1 and NOVA1 in an infant with microcephaly, seizures and severe developmental delayH Fryssira, E Tsoutsou, S Psoni, et al.Cytogenetic and Genome Research|May 9, 2013
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 rearrangementE Manolakos, A Vetro, E Papadopoulou, et al.Cytogenetic and Genome Research|April 11, 2012
Tetrasomy 9p mosaicism associated with a normal phenotype in two casesI Papoulidis, M Kontodiou, M Tzimina, et al.Molecular Medicine Reports|April 8, 2011
Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridizationE Manolakos, K Kefalas, R Neroutsou, et al.Pageof 1