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Browsing by Author Weise, A.

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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-
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 reportManolakos, 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-
Showing results 1 to 2 of 2