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P N Ray

Showing results (31-40 of 110) with videos related to

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Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Analysis of an X-autosome translocation responsible for X-linked muscular dystrophyR G Worton, P N Ray, S Bodrug, et al.
Human Molecular Genetics|October 1, 1996
Expression of the dystrophin isoform Dp71 in differentiating human fetal myogenic culturesC N Tennyson, G Y Dally, P N Ray, et al.
Molecular and Cellular Biology|May 1, 1986
Molecular cloning of cDNA for rat argininosuccinate lyase and its expression in rat hepatoma cell linesM A Lambert, L R Simard, P N Ray, et al.
Neurology|September 25, 1998
Congenital cytoplasmic body myopathy with survival motor neuron gene deletion or Werdnig-Hoffmann diseaseJ Vajsar, T Balslev, P N Ray, et al.
Clinical Genetics|December 9, 2009
Direct-to-consumer genetic testing: good, bad or benign?T Caulfield, N M Ries, P N Ray, et al.
Journal of Medical Genetics|December 1, 1986
Molecular deletion analysis in Duchenne muscular dystrophyN S Thomas, P N Ray, R G Worton, et al.
Human Mutation|February 6, 1998
A 3-base pair insertional mutation in the choroideremia geneN Nesslinger, S Horrocks, P N Ray, et al.
Journal of Medical Genetics|August 1, 1997
Monozygotic twins discordant for Aicardi syndromeT Costa, W Greer, G Rysiecki, et al.
Journal of Intellectual Disability Research : JIDR|December 7, 2011
Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndromeG Costain, E W C Chow, P N Ray, et al.
Molecular and Cellular Biology|January 1, 1990
Molecular and functional analysis of the muscle-specific promoter region of the Duchenne muscular dystrophy geneH J Klamut, S B Gangopadhyay, R G Worton, et al.
Pageof 11

Showing results (31-40 of 110) with videos related to

Sort By:
Pageof 11
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Analysis of an X-autosome translocation responsible for X-linked muscular dystrophyR G Worton, P N Ray, S Bodrug, et al.
Human Molecular Genetics|October 1, 1996
Expression of the dystrophin isoform Dp71 in differentiating human fetal myogenic culturesC N Tennyson, G Y Dally, P N Ray, et al.
Molecular and Cellular Biology|May 1, 1986
Molecular cloning of cDNA for rat argininosuccinate lyase and its expression in rat hepatoma cell linesM A Lambert, L R Simard, P N Ray, et al.
Neurology|September 25, 1998
Congenital cytoplasmic body myopathy with survival motor neuron gene deletion or Werdnig-Hoffmann diseaseJ Vajsar, T Balslev, P N Ray, et al.
Clinical Genetics|December 9, 2009
Direct-to-consumer genetic testing: good, bad or benign?T Caulfield, N M Ries, P N Ray, et al.
Journal of Medical Genetics|December 1, 1986
Molecular deletion analysis in Duchenne muscular dystrophyN S Thomas, P N Ray, R G Worton, et al.
Human Mutation|February 6, 1998
A 3-base pair insertional mutation in the choroideremia geneN Nesslinger, S Horrocks, P N Ray, et al.
Journal of Medical Genetics|August 1, 1997
Monozygotic twins discordant for Aicardi syndromeT Costa, W Greer, G Rysiecki, et al.
Journal of Intellectual Disability Research : JIDR|December 7, 2011
Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndromeG Costain, E W C Chow, P N Ray, et al.
Molecular and Cellular Biology|January 1, 1990
Molecular and functional analysis of the muscle-specific promoter region of the Duchenne muscular dystrophy geneH J Klamut, S B Gangopadhyay, R G Worton, et al.
Pageof 11