1. Repository of OAI
Ελληνικά   English  

Browsing by Author Kitsiou-Tzeli, S.

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Jump to: Α Β Γ Δ Ε Ζ Η Θ Ι Κ Λ Μ Ν Ξ Ο Π Ρ Σ Τ Υ Φ Χ Ψ Ω
or enter first few letters:  
View Option
Showing results 1 to 5 of 5
TitleAuthor(s)Issue date???itemlist.???
Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridizationManolakos, E.; Kefalas, K.; Neroutsou, R.; Lagou, M.; Kosyakova, N.; Ewers, E.; Ziegler, M.; Weise, A.; Tsoplou, P.; Rapti, S. M.; Papoulidis, I.; Anastasakis, E.; Garas, A.; Sotiriou, S.; Eleftheriades, M.; Peitsidis, P.; Malathrakis, D.; Thomaidis, L.; Kitsos, G.; Orru, S.; Liehr, T.; Petersen, M. B.; Kitsiou-Tzeli, S.24-Nov-2015-
Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boyManolakos, E.; Sarri, C.; Vetro, A.; Kefalas, K.; Leze, E.; Sofocleus, C.; Kitsos, G.; Merou, K.; Kokotas, H.; Papadopoulou, A.; Attilakos, A.; Petersen, M. B.; Kitsiou-Tzeli, S.24-Nov-2015-
FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formationKoumbaris, G.; Hatzisevastou-Loukidou, H.; Alexandrou, A.; Ioannides, M.; Christodoulou, C.; Fitzgerald, T.; Rajan, D.; Clayton, S.; Kitsiou-Tzeli, S.; Vermeesch, J. R.; Skordis, N.; Antoniou, P.; Kurg, A.; Georgiou, I.; Carter, N. P.; Patsalis, P. C.24-Nov-2015-
Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1Thienpont, B.; Dimitriadou, E.; Theodoropoulos, K.; Breckpot, J.; Fryssira, H.; Kitsiou-Tzeli, S.; Tzoufi, M.; Vermeesch, J. R.; Syrrou, M.; Devriendt, K.24-Nov-2015-
Supernumerary marker chromosomes (SMCs) in Turner syndrome are mostly derived from the Y chromosomePatsalis, P. C.; Hadjimarcou, M. I.; Velissariou, V.; Kitsiou-Tzeli, S.; Zera, C.; Syrrou, M.; Lyberatou, E.; Tsezou, A.; Galla, A.; Skordis, N.24-Nov-2015-
Showing results 1 to 5 of 5