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J M Vance

Showing results (11-20 of 104) with videos related to

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Neurology|August 10, 2005
Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutationsD Zhu, M L Kennerson, G Walizada, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|June 1, 1996
Ocular motility in North Carolina autosomal dominant ataxiaK W Small, S C Pollock, J M Vance, et al.
FEBS Letters|December 9, 1996
Toxicity of expanded polyglutamine-domain proteins in Escherichia coliO Onodera, A D Roses, S Tsuji, et al.
American Journal of Medical Genetics|February 1, 1985
Segregation and linkage analysis of alpha-N-acetyl-D-glucosaminidase (NAG) levels in a black familyM A Pericak-Vance, J M Vance, R C Elston, et al.
Annals of Human Genetics|March 29, 2007
Investigation of the PARK10 gene in Parkinson diseaseY J Li, J Deng, G M Mayhew, et al.
Neurology|February 9, 2005
Family-based case-control study of cigarette smoking and Parkinson diseaseW K Scott, F Zhang, J M Stajich, et al.
Molecular Vision|June 27, 2000
Physical and genetic mapping of the macular corneal dystrophy locus on chromosome 16q and exclusion of TAT and LCAT as candidate genesN P Liu, S Dew-Knight, F Jonasson, et al.
Nucleic Acids Research|May 11, 1994
Partitioned pulsed-field gel electrophoresis-PCR (PPF-PCR): a new method for pulsed-field mapping for STS and microsatellitesP H Denton, J B Cullen, D Loeb, et al.
Genomics|July 1, 1992
North Carolina macular dystrophy is assigned to chromosome 6K W Small, J L Weber, A Roses, et al.
Lancet (London, England)|December 17, 1994
Dentatorubral-pallidoluysian atrophy and Haw River syndromeJ R Burke, T Ikeuchi, R Koide, et al.
Pageof 11

Showing results (11-20 of 104) with videos related to

Sort By:
Pageof 11
Neurology|August 10, 2005
Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutationsD Zhu, M L Kennerson, G Walizada, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|June 1, 1996
Ocular motility in North Carolina autosomal dominant ataxiaK W Small, S C Pollock, J M Vance, et al.
FEBS Letters|December 9, 1996
Toxicity of expanded polyglutamine-domain proteins in Escherichia coliO Onodera, A D Roses, S Tsuji, et al.
American Journal of Medical Genetics|February 1, 1985
Segregation and linkage analysis of alpha-N-acetyl-D-glucosaminidase (NAG) levels in a black familyM A Pericak-Vance, J M Vance, R C Elston, et al.
Annals of Human Genetics|March 29, 2007
Investigation of the PARK10 gene in Parkinson diseaseY J Li, J Deng, G M Mayhew, et al.
Neurology|February 9, 2005
Family-based case-control study of cigarette smoking and Parkinson diseaseW K Scott, F Zhang, J M Stajich, et al.
Molecular Vision|June 27, 2000
Physical and genetic mapping of the macular corneal dystrophy locus on chromosome 16q and exclusion of TAT and LCAT as candidate genesN P Liu, S Dew-Knight, F Jonasson, et al.
Nucleic Acids Research|May 11, 1994
Partitioned pulsed-field gel electrophoresis-PCR (PPF-PCR): a new method for pulsed-field mapping for STS and microsatellitesP H Denton, J B Cullen, D Loeb, et al.
Genomics|July 1, 1992
North Carolina macular dystrophy is assigned to chromosome 6K W Small, J L Weber, A Roses, et al.
Lancet (London, England)|December 17, 1994
Dentatorubral-pallidoluysian atrophy and Haw River syndromeJ R Burke, T Ikeuchi, R Koide, et al.
Pageof 11