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Gerth-Kahlert C, Koller S (2018) Ciliopathies. Klin Monbl Augenheilkd235:264-272
Gerth-Kahlert C, Maggi J,Toteberg-Harms M, Tiwari A, Budde B, Nürnberg P, Koller S, Berger W (2018) Absence of goniodysgenesis in patients with chromosome 13q microdeletion-related microcoria. Ophthalmol Glaucoma 1:145-147
Gerth-Kahlert C, Tiwari A, Hauri-Hohl MM, Hanson JVM, Bahr A, Palmowski-Wolfe A, Güngör T, Berger W (2018) Unusual retinopathy in a child with severe combined immune deficiency. Ophthalmic Genet 39:92-94
Neubauer J, Lecca MR, Russo G, Bartsch C, Medeiros-Domingo A, Berger W, Haas C (2018) Exome analysis in 34 sudden unexplained death (SUD) victims mainly identified variants in channelopathy-associated genes. Int J Legal Med132:1057-1065
Valomon A, Holst SC, Borrello A, Weigend S, Müller T, Berger W, Sommerauer M, Baumann CR, Landolt HP (2018) Effects of COMT genotype and tolcapone on lapses of sustained attention after sleep deprivation in healthy young men. Neuropsychopharmacology 43:1599-1607
