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W B Dobyns

Showing results (41-50 of 151) with videos related to

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American Journal of Medical Genetics|December 1, 1993
Familial remitting chorea, nystagmus, and cataractsP G Wheeler, W B Dobyns, D A Plager, et al.
American Journal of Medical Genetics|May 14, 1999
Microcephaly with simplified gyral pattern in six related childrenA Peiffer, N Singh, M Leppert, et al.
Pediatric Neurology|October 1, 1996
Autosomal dominant torsion dystonia with onset in infancyS H Mostofsky, P A Blasco, I J Butler, et al.
Neuropediatrics|December 19, 2003
Characterization of brain malformations in the Baraitser-Winter syndrome and review of the literatureM Rossi, R Guerrini, W B Dobyns, et al.
Human Genetics|January 1, 1984
New chromosomal syndrome: Miller-Dieker syndrome and monosomy 17p13R F Stratton, W B Dobyns, S D Airhart, et al.
Annals of Neurology|April 18, 1998
Cerebrospinal fluid homovanillic acid levels in rapid-onset dystonia-parkinsonismA Brashear, I J Butler, K Hyland, et al.
Mechanisms of Development|March 23, 2000
Lissencephaly associated mutations suggest a requirement for the PAFAH1B heterotrimeric complex in brain developmentK J Sweeney, G D Clark, A Prokscha, et al.
Pediatric Neurology|September 1, 1995
Congenital muscular dystrophies: clinical review and proposed classificationE Parano, L Pavone, A Fiumara, et al.
American Journal of Human Genetics|March 1, 1991
Clinical and molecular diagnosis of Miller-Dieker syndromeW B Dobyns, C J Curry, H E Hoyme, et al.
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.
Pageof 16

Showing results (41-50 of 151) with videos related to

Sort By:
Pageof 16
American Journal of Medical Genetics|December 1, 1993
Familial remitting chorea, nystagmus, and cataractsP G Wheeler, W B Dobyns, D A Plager, et al.
American Journal of Medical Genetics|May 14, 1999
Microcephaly with simplified gyral pattern in six related childrenA Peiffer, N Singh, M Leppert, et al.
Pediatric Neurology|October 1, 1996
Autosomal dominant torsion dystonia with onset in infancyS H Mostofsky, P A Blasco, I J Butler, et al.
Neuropediatrics|December 19, 2003
Characterization of brain malformations in the Baraitser-Winter syndrome and review of the literatureM Rossi, R Guerrini, W B Dobyns, et al.
Human Genetics|January 1, 1984
New chromosomal syndrome: Miller-Dieker syndrome and monosomy 17p13R F Stratton, W B Dobyns, S D Airhart, et al.
Annals of Neurology|April 18, 1998
Cerebrospinal fluid homovanillic acid levels in rapid-onset dystonia-parkinsonismA Brashear, I J Butler, K Hyland, et al.
Mechanisms of Development|March 23, 2000
Lissencephaly associated mutations suggest a requirement for the PAFAH1B heterotrimeric complex in brain developmentK J Sweeney, G D Clark, A Prokscha, et al.
Pediatric Neurology|September 1, 1995
Congenital muscular dystrophies: clinical review and proposed classificationE Parano, L Pavone, A Fiumara, et al.
American Journal of Human Genetics|March 1, 1991
Clinical and molecular diagnosis of Miller-Dieker syndromeW B Dobyns, C J Curry, H E Hoyme, et al.
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.
Pageof 16