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Epilepsy Research|October 9, 1999
Detecting genes in new and old mouse models for epilepsy: a prospectus through the magnifying glassW N FrankelHuman Molecular Genetics|September 2, 1999
Ataxic mouse mutants and molecular mechanisms of absence epilepsyC F Fletcher, W N FrankelNature Genetics|August 10, 2000
The roads from phenotypic variation to gene discovery: mutagenesis versus QTLsJ H Nadeau, W N FrankelMammalian Genome : Official Journal of the International Mammalian Genome Society|August 1, 1994
Mapping of mouse intracisternal A-particle proviral markers in an interspecific backcrossK K Lueders, W N FrankelMammalian Genome : Official Journal of the International Mammalian Genome Society|May 1, 1994
Endogenous nonecotropic proviruses mapped with oligonucleotide probes from the long terminal repeat regionW N Frankel, J M CoffinGenomics|November 23, 2000
Multiple seizure susceptibility genes on chromosome 7 in SWXL-4 congenic mouse strainsM E Legare, W N FrankelGenes, Brain, and Behavior|January 28, 2009
Genetic complexity of absence seizures in substrains of C3H miceS Tokuda, B J Beyer, W N FrankelNeuron|January 12, 1999
Identification of the mouse neuromuscular degeneration gene and mapping of a second site suppressor alleleG A Cox, C L Mahaffey, W N FrankelPageof 10