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R L Nussbaum

Showing results (71-80 of 115) with videos related to

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The EMBO Journal|June 1, 1995
FXR1, an autosomal homolog of the fragile X mental retardation geneM C Siomi, H Siomi, W H Sauer, et al.
Molecular Genetics and Metabolism|June 17, 2006
The effect of missense mutations in the RhoGAP-homology domain on ocrl1 functionU Lichter-Konecki, L W Farber, J S Cronin, et al.
American Journal of Human Genetics|November 1, 1985
Thymidylate synthase-deficient Chinese hamster cells: a selection system for human chromosome 18 and experimental system for the study of thymidylate synthase regulation and fragile X expressionR L Nussbaum, R M Walmsley, J G Lesko, et al.
Ophthalmology|August 1, 1984
The Gardner syndrome. Significance of ocular featuresR A Lewis, W E Crowder, L A Eierman, et al.
Journal of Medical Genetics|December 14, 2004
Parkinsonism among Gaucher disease carriersO Goker-Alpan, R Schiffmann, M E LaMarca, et al.
Journal of Neurochemistry|July 22, 2005
Fatty acid incorporation is decreased in astrocytes cultured from alpha-synuclein gene-ablated miceP I Castagnet, M Y Golovko, G C Barceló-Coblijn, et al.
Human Genetics|September 16, 1998
Identification, localization and characterization of the human gamma-synuclein geneC Lavedan, E Leroy, A Dehejia, 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.
Genomics|April 1, 1991
Linkage analysis in X-linked ocular albinismR E Schnur, R L Nussbaum, L Anson-Cartwright, et al.
American Journal of Human Genetics|February 1, 1986
New mutation and prenatal diagnosis in ornithine transcarbamylase deficiencyR L Nussbaum, B A Boggs, A L Beaudet, et al.
Pageof 12

Showing results (71-80 of 115) with videos related to

Sort By:
Pageof 12
The EMBO Journal|June 1, 1995
FXR1, an autosomal homolog of the fragile X mental retardation geneM C Siomi, H Siomi, W H Sauer, et al.
Molecular Genetics and Metabolism|June 17, 2006
The effect of missense mutations in the RhoGAP-homology domain on ocrl1 functionU Lichter-Konecki, L W Farber, J S Cronin, et al.
American Journal of Human Genetics|November 1, 1985
Thymidylate synthase-deficient Chinese hamster cells: a selection system for human chromosome 18 and experimental system for the study of thymidylate synthase regulation and fragile X expressionR L Nussbaum, R M Walmsley, J G Lesko, et al.
Ophthalmology|August 1, 1984
The Gardner syndrome. Significance of ocular featuresR A Lewis, W E Crowder, L A Eierman, et al.
Journal of Medical Genetics|December 14, 2004
Parkinsonism among Gaucher disease carriersO Goker-Alpan, R Schiffmann, M E LaMarca, et al.
Journal of Neurochemistry|July 22, 2005
Fatty acid incorporation is decreased in astrocytes cultured from alpha-synuclein gene-ablated miceP I Castagnet, M Y Golovko, G C Barceló-Coblijn, et al.
Human Genetics|September 16, 1998
Identification, localization and characterization of the human gamma-synuclein geneC Lavedan, E Leroy, A Dehejia, 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.
Genomics|April 1, 1991
Linkage analysis in X-linked ocular albinismR E Schnur, R L Nussbaum, L Anson-Cartwright, et al.
American Journal of Human Genetics|February 1, 1986
New mutation and prenatal diagnosis in ornithine transcarbamylase deficiencyR L Nussbaum, B A Boggs, A L Beaudet, et al.
Pageof 12