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Browsing by Author Aperis, G.

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Showing results 1 to 4 of 4

Title	Author(s)	Issue date	???itemlist.???
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	-
A large GLC1C Greek family with a myocilin T377M mutation: inheritance and phenotypic variability	Petersen, M. B.; Kitsos, G.; Samples, J. R.; Gaudette, N. D.; Economou-Petersen, E.; Sykes, R.; Rust, K.; Grigoriadou, M.; Aperis, G.; Choi, D.; Psilas, K.; Craig, J. E.; Kramer, P. L.; Mackey, D. A.; Wirtz, M. K.	24-Nov-2015	-
A novel locus on 19q13 associated with autosomal-dominant macular dystrophy in a large Greek family	Yang, Z.; Kitsos, G.; Tong, Z.; Payne, M.; Gorezis, S.; Psilas, K.; Grigoriadou, M.; Zhao, Y.; Kamaya, S.; Aperis, G.; Petersen, M. B.; Zhang, K.	24-Nov-2015	-
Refining the primary open-angle glaucoma GLC1C region on chromosome 3 by haplotype analysis	Samples, J. R.; Kitsos, G.; Economou-Petersen, E.; Steinkamp, P.; Sykes, R.; Rust, K.; Patzer, C.; Grigoriadou, M.; Aperis, G.; Psilas, K.; Petersen, M. B.; Wirtz, M. K.	24-Nov-2015	-

Showing results 1 to 4 of 4