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Browsing by Author Kokotas, H.

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Showing results 1 to 3 of 3
TitleAuthor(s)Issue date???itemlist.???
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-
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-
Primary open angle glaucoma due to T377M MYOC: Population mapping of a Greek founder mutation in Northwestern GreeceKitsos, G.; Petrou, Z.; Grigoriadou, M.; Samples, J. R.; Hewitt, A. W.; Kokotas, H.; Giannoulia-Karantana, A.; Mackey, D. A.; Wirtz, M. K.; Moschou, M.; Ioannidis, J. P.; Petersen, M. B.24-Nov-2015-
Showing results 1 to 3 of 3