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W N Frankel

Showing results (51-60 of 82) with videos related to

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Genomics|May 15, 2001
High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and Waltzer (Cdh23v)E C Bryda, H J Kim, M E Legare, et al.
Genes, Brain, and Behavior|September 25, 2014
A genetic interaction network model of a complex neurological diseaseA L Tyler, T C McGarr, B J Beyer, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 26, 2000
A new spontaneous mouse mutation in the Kcne1 geneV A Letts, A Valenzuela, C Dunbar, et al.
Genes, Brain, and Behavior|July 13, 2011
Etiology of a genetically complex seizure disorder in Celf4 mutant miceJ L Wagnon, C L Mahaffey, W Sun, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
The AXB and BXA set of recombinant inbred mouse strainsJ D Marshall, J L Mu, Y C Cheah, et al.
Genomics|July 1, 1997
Genetic and physical maps of the stargazer locus on mouse chromosome 15V A Letts, A Valenzuela, J P Kirley, et al.
Mutation Research|April 1, 1993
Molecular analysis of viable spontaneous and radiation-induced albino (c)-locus mutations in the mouseE M Rinchik, J P Stoye, W N Frankel, et al.
Nature Genetics|April 1, 1994
Multifactorial inheritance of neural tube defects: localization of the major gene and recognition of modifiers in ct mutant miceP E Neumann, W N Frankel, V A Letts, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 1, 1995
New seizure frequency QTL and the complex genetics of epilepsy in EL miceW N Frankel, A Valenzuela, C M Lutz, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1993
Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesteraseC Bowes, T Li, W N Frankel, et al.
Pageof 9

Showing results (51-60 of 82) with videos related to

Sort By:
Pageof 9
Genomics|May 15, 2001
High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and Waltzer (Cdh23v)E C Bryda, H J Kim, M E Legare, et al.
Genes, Brain, and Behavior|September 25, 2014
A genetic interaction network model of a complex neurological diseaseA L Tyler, T C McGarr, B J Beyer, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 26, 2000
A new spontaneous mouse mutation in the Kcne1 geneV A Letts, A Valenzuela, C Dunbar, et al.
Genes, Brain, and Behavior|July 13, 2011
Etiology of a genetically complex seizure disorder in Celf4 mutant miceJ L Wagnon, C L Mahaffey, W Sun, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
The AXB and BXA set of recombinant inbred mouse strainsJ D Marshall, J L Mu, Y C Cheah, et al.
Genomics|July 1, 1997
Genetic and physical maps of the stargazer locus on mouse chromosome 15V A Letts, A Valenzuela, J P Kirley, et al.
Mutation Research|April 1, 1993
Molecular analysis of viable spontaneous and radiation-induced albino (c)-locus mutations in the mouseE M Rinchik, J P Stoye, W N Frankel, et al.
Nature Genetics|April 1, 1994
Multifactorial inheritance of neural tube defects: localization of the major gene and recognition of modifiers in ct mutant miceP E Neumann, W N Frankel, V A Letts, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 1, 1995
New seizure frequency QTL and the complex genetics of epilepsy in EL miceW N Frankel, A Valenzuela, C M Lutz, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1993
Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesteraseC Bowes, T Li, W N Frankel, et al.
Pageof 9