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J W Day

Showing results (21-30 of 45) with videos related to

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Cytogenetic and Genome Research|October 4, 2003
Molecular genetics of spinocerebellar ataxia type 8 (SCA8)A K Mosemiller, J C Dalton, J W Day, et al.
The Journal of Urology|April 1, 1981
In vitro chemotherapeutic testing of urologic tumorsJ W Day, S Shrivastav, G Lin, et al.
Genome Dynamics|August 30, 2008
Dominant non-coding repeat expansions in human diseaseK A Dick, J M Margolis, J W Day, et al.
Neuromuscular Disorders : NMD|March 4, 1999
Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2)J W Day, R Roelofs, B Leroy, et al.
Nature Genetics|June 10, 1998
Genetic mapping of a second myotonic dystrophy locusL P Ranum, P F Rasmussen, K A Benzow, et al.
Neurology|September 12, 2000
Spinocerebellar ataxia type 8: clinical features in a large familyJ W Day, L J Schut, M L Moseley, et al.
Eating and Weight Disorders : EWD|December 15, 2010
Targeting parents for the treatment of pediatric obesity in boys with Duchenne muscular dystrophy: a case seriesA Arikian, K Boutelle, C B Peterson, et al.
Human Genetics|February 14, 2007
Gene symbol: SCN8A. Disease: Ataxia. Accession #Hd0520M H Meisler, M M Trudeau, J C Dalton, et al.
Journal of Medical Genetics|October 21, 2005
Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardationM M Trudeau, J C Dalton, J W Day, et al.
Synapse (New York, N.Y.)|February 12, 1998
Desensitization of mutant acetylcholine receptors in transgenic mice reduces the amplitude of neuromuscular synaptic currentsB J Bhattacharyya, J W Day, J E Gundeck, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Cytogenetic and Genome Research|October 4, 2003
Molecular genetics of spinocerebellar ataxia type 8 (SCA8)A K Mosemiller, J C Dalton, J W Day, et al.
The Journal of Urology|April 1, 1981
In vitro chemotherapeutic testing of urologic tumorsJ W Day, S Shrivastav, G Lin, et al.
Genome Dynamics|August 30, 2008
Dominant non-coding repeat expansions in human diseaseK A Dick, J M Margolis, J W Day, et al.
Neuromuscular Disorders : NMD|March 4, 1999
Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2)J W Day, R Roelofs, B Leroy, et al.
Nature Genetics|June 10, 1998
Genetic mapping of a second myotonic dystrophy locusL P Ranum, P F Rasmussen, K A Benzow, et al.
Neurology|September 12, 2000
Spinocerebellar ataxia type 8: clinical features in a large familyJ W Day, L J Schut, M L Moseley, et al.
Eating and Weight Disorders : EWD|December 15, 2010
Targeting parents for the treatment of pediatric obesity in boys with Duchenne muscular dystrophy: a case seriesA Arikian, K Boutelle, C B Peterson, et al.
Human Genetics|February 14, 2007
Gene symbol: SCN8A. Disease: Ataxia. Accession #Hd0520M H Meisler, M M Trudeau, J C Dalton, et al.
Journal of Medical Genetics|October 21, 2005
Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardationM M Trudeau, J C Dalton, J W Day, et al.
Synapse (New York, N.Y.)|February 12, 1998
Desensitization of mutant acetylcholine receptors in transgenic mice reduces the amplitude of neuromuscular synaptic currentsB J Bhattacharyya, J W Day, J E Gundeck, et al.
Pageof 5