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Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 1996
Variable phenotype of rapid-onset dystonia-parkinsonismA Brashear, M R Farlow, I J Butler, et al.Molecular Medicine Today|June 22, 2000
Lissencephaly and subcortical band heterotopia: molecular basis and diagnosisR J Leventer, D T Pilz, N Matsumoto, et al.Neurology|September 30, 2005
A developmental and genetic classification for malformations of cortical developmentA J Barkovich, R I Kuzniecky, G D Jackson, et al.American Journal of Medical Genetics|September 24, 1999
X-linked lissencephaly with absent corpus callosum and ambiguous genitaliaW B Dobyns, E Berry-Kravis, N J Havernick, et al.American Journal of Medical Genetics|December 14, 1999
Familial lissencephaly with cleft palate and severe cerebellar hypoplasiaB Kerner, J M Graham, J A Golden, et al.Neurology|January 12, 2002
Classification system for malformations of cortical development: update 2001A J Barkovich, R I Kuzniecky, G D Jackson, et al.American Journal of Human Genetics|October 1, 1991
Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridizationA Kuwano, S A Ledbetter, W B Dobyns, et al.Laboratory Investigation; a Journal of Technical Methods and Pathology|January 1, 1977
Glycogen complexes in muscle in Reye's syndrome simulating virus-like particlesD N Collins, E F GilbertArchives of Pathology & Laboratory Medicine|March 1, 1987
Mesenteric cyst-ovarian implant syndromeH M Payan, E F GilbertArchives of Pathology & Laboratory Medicine|February 1, 1979
Angiosarcoma complicating generalized lymphangiectasiaK T Chen, E F GilbertPageof 40