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W B Dobyns

Showing results (61-70 of 151) with videos related to

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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.
Journal of Neurology|October 1, 1996
Olivopontocerebellar atrophy leading to recognition of carbohydrate-deficient glycoprotein syndrome type IL Pavone, A Fiumara, R Barone, et al.
Neurology|April 1, 1997
Rapid-onset dystonia-parkinsonism in a second familyA Brashear, D DeLeon, S B Bressman, et al.
Neurology|July 1, 1992
Causal heterogeneity in isolated lissencephalyW B Dobyns, E R Elias, A C Newlin, et al.
Pediatric Neurology|January 1, 1990
Plasmapheresis with acute inflammatory polyneuropathyB O Khatri, J R Flamini, J K Baruah, et al.
Human Mutation|January 1, 1997
Mutations and polymorphisms in the tuberous sclerosis complex gene on chromosome 16K S Au, J A Rodriguez, E Rodriguez, et al.
American Journal of Medical Genetics|May 3, 1996
Diffuse polymicrogyria associated with an unusual pattern of multiple congenital anomalies including turribrachycephaly and hypogenitalismR D Cohn, G Gillessen-Kaesbach, W B Dobyns, et al.
The Journal of Pediatrics|April 1, 1983
Miller-Dieker syndrome: lissencephaly and monosomy 17pW B Dobyns, R F Stratton, J T Parke, et al.
Neuropediatrics|April 1, 1996
A classification scheme for malformations of cortical developmentA J Barkovich, R I Kuzniecky, W B Dobyns, et al.
Science (New York, N.Y.)|May 20, 2006
Comment on "The Brain of LB1, Homo floresiensis"R D Martin, A M Maclarnon, J L Phillips, et al.
Pageof 16

Showing results (61-70 of 151) with videos related to

Sort By:
Pageof 16
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.
Journal of Neurology|October 1, 1996
Olivopontocerebellar atrophy leading to recognition of carbohydrate-deficient glycoprotein syndrome type IL Pavone, A Fiumara, R Barone, et al.
Neurology|April 1, 1997
Rapid-onset dystonia-parkinsonism in a second familyA Brashear, D DeLeon, S B Bressman, et al.
Neurology|July 1, 1992
Causal heterogeneity in isolated lissencephalyW B Dobyns, E R Elias, A C Newlin, et al.
Pediatric Neurology|January 1, 1990
Plasmapheresis with acute inflammatory polyneuropathyB O Khatri, J R Flamini, J K Baruah, et al.
Human Mutation|January 1, 1997
Mutations and polymorphisms in the tuberous sclerosis complex gene on chromosome 16K S Au, J A Rodriguez, E Rodriguez, et al.
American Journal of Medical Genetics|May 3, 1996
Diffuse polymicrogyria associated with an unusual pattern of multiple congenital anomalies including turribrachycephaly and hypogenitalismR D Cohn, G Gillessen-Kaesbach, W B Dobyns, et al.
The Journal of Pediatrics|April 1, 1983
Miller-Dieker syndrome: lissencephaly and monosomy 17pW B Dobyns, R F Stratton, J T Parke, et al.
Neuropediatrics|April 1, 1996
A classification scheme for malformations of cortical developmentA J Barkovich, R I Kuzniecky, W B Dobyns, et al.
Science (New York, N.Y.)|May 20, 2006
Comment on "The Brain of LB1, Homo floresiensis"R D Martin, A M Maclarnon, J L Phillips, et al.
Pageof 16