An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4

Por Selenti, Nikoletta, Tzetis, Maria, Braoudaki, Maria, Gianikou, Krinio, Kitsiou-Tzeli, Sofia, Fryssira, Helen
Publicado no Mol Cytogenet (2015)

Erratum to: An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4

Por Selenti, Nikoletta, Tzetis, Maria, Braoudaki, Maria, Giannikou, Krinio, Kitsiou-Tzeli, Sofia, Fryssira, Helen
Publicado no Mol Cytogenet (2015)

Survivin regulation by HER2 through NF-κB and c-myc in irradiated breast cancer cells

Por Papanikolaou, Vassilis, Iliopoulos, Dimitrios, Dimou, Ioannis, Dubos, Stephanie, Kappas, Constantine, Kitsiou-Tzeli, Sofia, Tsezou, Aspasia
Publicado em 2011

Influence of Interleukin 1α (IL-1α), IL-4, and IL-6 Polymorphisms on Genetic Susceptibility to Chronic Osteomyelitis

Por Tsezou, Aspasia, Poultsides, Lazaros, Kostopoulou, Fotini, Zintzaras, Elias, Satra, Maria, Kitsiou-Tzeli, Sofia, Malizos, Konstantinos N.
Publicado em 2008

Genomic screening of ABCA4 and array CGH analysis underline the genetic variability of Greek patients with inherited retinal diseases

Por Tsipi, Maria, Tzetis, Maria, Kosma, Konstantina, Moschos, Marilita, Braoudaki, Maria, Poulou, Myrto, Kanavakis, Emmanuel, Kitsiou-Tzeli, Sofia
Publicado no Meta Gene (2016)

Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype

Por Sismani, Carolina, Kitsiou-Tzeli, Sofia, Ioannides, Marios, Christodoulou, Christodoulos, Anastasiadou, Violetta, Stylianidou, Goula, Papadopoulou, Eleftheria, Kanavakis, Emanuel, Kosmaidou-Aravidou, Zoe, Patsalis, Philippos C
Publicado em 2008

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

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

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

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

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

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

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

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