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J A Trofatter

Showing results (11-20 of 41) with videos related to

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Genomics|August 1, 1996
Cloning and characterization of a novel human clathrin heavy chain gene (CLTCL)K R Long, J A Trofatter, V Ramesh, et al.
American Journal of Medical Genetics|June 1, 1992
New variant in exon 3 of the proteolipid protein (PLP) gene in a family with Pelizaeus-Merzbacher diseaseV M Pratt, J A Trofatter, M B Larsen, et al.
Human Molecular Genetics|March 1, 1994
The murine NF2 homologue encodes a highly conserved merlin protein with alternative formsV H Haase, J A Trofatter, M MacCollin, et al.
American Journal of Human Genetics|July 1, 1991
A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genesC U Kirchgessner, J A Trofatter, M M Mahtani, et al.
Journal of Biological Rhythms|December 12, 2003
New quantitative trait loci for the genetic variance in circadian period of locomotor activity between inbred strains of miceJ R Hofstetter, J A Trofatter, K L Kernek, et al.
Journal of Medical Genetics|April 1, 1993
Onset symptoms in 510 patients with Huntington's diseaseL Di Maio, F Squitieri, G Napolitano, et al.
Journal of Medical Genetics|April 1, 1993
Suicide risk in Huntington's diseaseL Di Maio, F Squitieri, G Napolitano, et al.
American Journal of Medical Genetics|January 1, 1991
A new mutation in the proteolipid protein (PLP) gene in a German family with Pelizaeus-Merzbacher diseaseV M Pratt, J A Trofatter, A Schinzel, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 15, 1993
Myelin protein zero gene mutated in Charcot-Marie-tooth type 1B patientsY Su, D G Brooks, L Li, et al.
Genome Research|October 1, 1995
An expression-independent catalog of genes from human chromosome 22J A Trofatter, K R Long, J R Murrell, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Genomics|August 1, 1996
Cloning and characterization of a novel human clathrin heavy chain gene (CLTCL)K R Long, J A Trofatter, V Ramesh, et al.
American Journal of Medical Genetics|June 1, 1992
New variant in exon 3 of the proteolipid protein (PLP) gene in a family with Pelizaeus-Merzbacher diseaseV M Pratt, J A Trofatter, M B Larsen, et al.
Human Molecular Genetics|March 1, 1994
The murine NF2 homologue encodes a highly conserved merlin protein with alternative formsV H Haase, J A Trofatter, M MacCollin, et al.
American Journal of Human Genetics|July 1, 1991
A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genesC U Kirchgessner, J A Trofatter, M M Mahtani, et al.
Journal of Biological Rhythms|December 12, 2003
New quantitative trait loci for the genetic variance in circadian period of locomotor activity between inbred strains of miceJ R Hofstetter, J A Trofatter, K L Kernek, et al.
Journal of Medical Genetics|April 1, 1993
Onset symptoms in 510 patients with Huntington's diseaseL Di Maio, F Squitieri, G Napolitano, et al.
Journal of Medical Genetics|April 1, 1993
Suicide risk in Huntington's diseaseL Di Maio, F Squitieri, G Napolitano, et al.
American Journal of Medical Genetics|January 1, 1991
A new mutation in the proteolipid protein (PLP) gene in a German family with Pelizaeus-Merzbacher diseaseV M Pratt, J A Trofatter, A Schinzel, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 15, 1993
Myelin protein zero gene mutated in Charcot-Marie-tooth type 1B patientsY Su, D G Brooks, L Li, et al.
Genome Research|October 1, 1995
An expression-independent catalog of genes from human chromosome 22J A Trofatter, K R Long, J R Murrell, et al.
Pageof 5