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Genomics|May 1, 1994
Evidence for the existence of a fourth dominantly inherited spinocerebellar ataxia locusI Lopes-Cendes, E Andermann, G A RouleauGenetic Epidemiology|January 1, 1987
Pedigree discriminant analysis of two French Canadian Tay-Sachs familiesB J Keats, R C Elston, E AndermannClinical Genetics|May 1, 1989
The mutation mechanism causing juvenile-onset Tay-Sachs disease among LebaneseP Hechtman, B Boulay, J Bayleran, et al.Neuropediatrics|November 9, 2000
Polymicrogyria and motor neuropathy in Micro syndromeM C Nassogne, B Henrot, C Saint-Martin, et al.Pediatric Neurology|February 1, 1994
Childhood stroke and lupus anticoagulantJ C Olson, R J Konkol, J C Gill, et al.American Journal of Medical Genetics|September 1, 1985
Syndromes with lissencephaly. II: Walker-Warburg and cerebro-oculo-muscular syndromes and a new syndrome with type II lissencephalyW B Dobyns, J B Kirkpatrick, H M Hittner, et al.Journal of Child Neurology|October 8, 1999
Clinical nosologic and genetic aspects of Joubert and related syndromesP F Chance, L Cavalier, D Satran, et al.Neuropharmacology|December 1, 1994
Potassium channel activators counteract anoxic hyperexcitability but not 4-aminopyridine-induced epileptiform activity in the rat hippocampal sliceD Mattia, T Nagao, M A Rogawski, et al.Neuroscience|January 1, 1982
Neuronal responses to putative neurotransmitters during penicillin epileptogenesisM Avoli, A Brancati, C Pacitti, et al.American Journal of Medical Genetics|September 1, 1985
Deficiency of chromosome 8p21.1----8pter: case report and review of the literatureW B Dobyns, G W Dewald, R O Carlson, et al.Pageof 64