Lissencephaly/Bibliography

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• Kerjan, G. & J.G. Gleeson (2007), "Genetic mechanisms underlying abnormal neuronal migration in classical lissencephaly", Trends in Genetics 23 (12): 623–630, DOI:10.1016/j.tig.2007.09.003 ^[e]
• Vallee, R.B. & J.W. Tsai (2006), "The cellular roles of the lissencephaly gene LIS1, and what they tell us about brain development", Genes Dev 20 (11): 1384–1393, DOI:10.1101/gad.1417206 ^[e]
• Ramirez, D.; E.J. Lammer & C.B. Johnson et al. (2004), "Autosomal recessive frontotemporal pachygyria", American Journal of Medical Genetics 124 (3): 231–238, DOI:10.1002/ajmg.a.20388 ^[e]
• Kurul, S.; H. Çakmakçi & E. Dirik (2004), "Agyria-pachygyria complex: MR findings and correlation with clinical features", Pediatric Neurology 30 (1): 16–23, DOI:10.1016/S0887-8994(03)00312-6 ^[e]
• Kato, Mitsuhiro & William B. Dobyns (2003), "Lissencephaly and the molecular basis of neuronal migration", Human Molecular Genetics 12 (Review Issue 1): 89–96, DOI:10.1093/hmg/ddg086 ^[e]
• Liang, J.S.; W.T. Lee & C. Young et al. (2002), "Agyria-pachygyria: Clinical, neuroimaging, and neurophysiologic correlations", Pediatric neurology 27 (3): 171–176, DOI:10.1016/S0887-8994(02)00401-0 ^[e]
• Hager, B.C.; I.Z. Dyme & S.R. Guertin et al. (1991), "Linear nevus sebaceous syndrome: megalencephaly and heterotopic grey matter", Pediatr Neurol 7 (1): 45–9, DOI:10.1016/0887-8994(91)90105-T
• Barkovich, A.J.; T.K. Koch & C.L. Carrol (1991), "The spectrum of lissencephaly: report of ten patients analyzed by magnetic resonance imaging", Ann Neurol 30 (2): 139–46, DOI:10.1002/ana.410300204