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Journal of Neurogenetics|January 1, 1987
Clinical and electrophysiological studies in a patient with keratitis, ichthyosis and deafness (KID) syndromeL G Chia, W M LiJournal of Neurogenetics|June 1, 1985
Mutant alleles at the locus elav in Drosophila melanogaster lead to nervous system defects. A developmental-genetic analysisA R Campos, D Grossman, K WhiteJournal of Neurogenetics|September 1, 1992
No-bridge of Drosophila melanogaster: portrait of a structural brain mutant of the central complexR Strauss, U Hanesch, M Kinkelin, et al.Journal of Neurogenetics|December 12, 2003
Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardationTamara Major, Biljana Culjkovic, Oliver Stojkovic, et al.Journal of Neurogenetics|December 12, 2003
Association analysis of 5-HTTLPR variants, 5-HT2a receptor gene 102T/C polymorphism and migraineGabriella Juhasz, Terezia Zsombok, Andras Laszik, et al.Journal of Neurogenetics|September 1, 1992
Identification and characterization of inebriated, a gene affecting neuronal excitability in DrosophilaM Stern, B GanetzkyJournal of Neurogenetics|August 1, 1987
Ultrastructure of the retina of Drosophila melanogaster: the mutant ora (outer rhabdomeres absent) and its inhibition of degeneration in rdgB (retinal degeneration-B)W S Stark, R SappJournal of Neurogenetics|January 1, 1987
Suppression of inherited muscle degeneration in a Drosophila mutant by mechanical and genetical immobilizationsK Kimura, T Shimozawa, T TanimuraJournal of Neurogenetics|July 6, 2017
Genetic approaches to retinal research in zebrafishStephanie Niklaus, Stephan C F NeuhaussPageof 79