Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-...

by Kokotas Haris, Orru Sandro, Mihalatos Markos, Weise Anja, Neroutsou Rozita, Thomaidis Loreta, Kosyakova Nadezda, Manolakos Emmanouil, Kitsos George, Liehr Thomas, Petersen Michael B
Published 2008-11-01

Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male

by Garas Antonios, Weise Anja, Ewers Elisabeth, Kosyakova Nadezda, Kontodiou Maria, Lagou Magdalini, Manolakos Emmanouil, Kitsiou-Tzeli Sofia, Orru Sandro, Liehr Thomas, Metaxotou Aikaterini
Published 2009-01-01

Prenatal diagnosis of Wolf-Hirschhorn syndrome confirmed by comparative genomic hybridization array: report of two cases and review of the literature

by Sifakis Stavros, Manolakos Emmanouil, Vetro Annalisa, Kappou Dimitra, Peitsidis Panagiotis, Kontodiou Maria, Garas Antonios, Vrachnis Nikolaos, Konstandinidou Anastasia, Zuffardi Orsetta, Orru Sandro, Papoulidis Ioannis
Published 2012-02-01

Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male

by Garas Antonios, Weise Anja, Ewers Elisabeth, Kosyakova Nadezda, Kontodiou Maria, Anagnostopoulou Katerina, Lagou Magdalini, Manolakos Emmanouil, Kitsiou-Tzeli Sofia, Orru Sandro, Liehr Thomas, Metaxotou Aikaterini
Published 2009-02-01

Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome)

by Peitsidis Panagiotis, Thomaidis Loretta, Papoulidis Ioannis, Louizou Eirini, Kefalas Konstantinos, Neroutsou Rosita, Orru Sandro, Manolakos Emmanouil, Sotiriou Sotirios, Kitsos George, Tsoplou Panagiota, Petersen Michael B, Metaxotou Aikaterini
Published 2009-12-01

Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy

by Papadopoulou Anna, Kokotas Haris, Merou Konstantina, Kitsos George, Sofocleus Christalena, Leze Eleni, Kefalas Konstantinos, Vetro Annalisa, Sarri Catherine, Manolakos Emmanouil, Attilakos Achilleas, Petersen Michael B, Kitsiou-Tzeli Sofia
Published 2011-04-01

Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy

by Papadopoulou Anna, Kokotas Haris, Merou Konstantina, Kitsos George, Sofocleus Christalena, Leze Eleni, Kefalas Konstantinos, Vetro Annalisa, Sarri Catherine, Manolakos Emmanouil, Attilakos Achilleas, Petersen Michael B, Kitsiou-Tzeli Sofia
Published 2011-02-01

The use of array-CGH in a cohort of Greek children with developmental delay

by Eleftheriades Makarios, Tsoplou Panagiota, Vasileiadis Lefteris, Kitsos George, Garas Antonios, Louizou Eirini, Rapti Stamatia-Maria, Kefalas Konstantinos, Vetro Annalisa, Manolakos Emmanouil, Peitsidis Panagiotis, Orru Sandro, Liehr Thomas, Petersen Michael B, Thomaidis Loretta
Published 2010-11-01