| Title | Author(s) | Issue date | ???itemlist.??? |
| 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, 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 boy | Manolakos, 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 | - |
| 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-CGH: Case report | Manolakos, E.; Kosyakova, N.; Thomaidis, L.; Neroutsou, R.; Weise, A.; Mihalatos, M.; Orru, S.; Kokotas, H.; Kitsos, G.; Liehr, T.; Petersen, M. B. | 24-Nov-2015 | - |
| 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, M. B. | 24-Nov-2015 | - |
| Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome) | Manolakos, E.; Orru, S.; Neroutsou, R.; Kefalas, K.; Louizou, E.; Papoulidis, I.; Thomaidis, L.; Peitsidis, P.; Sotiriou, S.; Kitsos, G.; Tsoplou, P.; Petersen, M. B.; Metaxotou, A. | 24-Nov-2015 | - |
| A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth | Papoulidis, I.; Manolakos, E.; Siomou, E.; Kefalas, K.; Thomaidis, L.; Liehr, T.; Vetro, A.; Athanasiadis, A.; Zuffardi, O.; Petersen, M. B. | 24-Nov-2015 | - |
| Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature | Manolakos, E.; Sifakis, S.; Sotiriou, S.; Peitsidis, P.; Eleftheriades, M.; Mersinias, V.; Liehr, T.; Thomaidis, L.; Kitsos, G.; Papoulidis, I.; Petersen, M. B.; Orru, S. | 24-Nov-2015 | - |
| The use of array-CGH in a cohort of Greek children with developmental delay | Manolakos, E.; Vetro, A.; Kefalas, K.; Rapti, S. M.; Louizou, E.; Garas, A.; Kitsos, G.; Vasileiadis, L.; Tsoplou, P.; Eleftheriades, M.; Peitsidis, P.; Orru, S.; Liehr, T.; Petersen, M. B.; Thomaidis, L. | 24-Nov-2015 | - |
