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S M Forrest

Showing results (21-30 of 48) with videos related to

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Nature|October 15, 1987
Preferential deletion of exons in Duchenne and Becker muscular dystrophiesS M Forrest, G S Cross, A Speer, et al.
Genomics|February 1, 1988
Further studies of gene deletions that cause Duchenne and Becker muscular dystrophiesS M Forrest, G S Cross, T Flint, et al.
Human Genetics|October 1, 1988
Patterns of exon deletions in Duchenne and Becker muscular dystrophyA P Read, R C Mountford, S M Forrest, et al.
British Medical Bulletin|July 1, 1989
Molecular analysis of Duchenne and Becker muscular dystrophiesD R Love, S M Forrest, T J Smith, et al.
Carbohydrate Research|June 26, 1992
Regioselectivity of the insertion reactions of some aromatic diazo compound complexes with cyclomaltoheptaoseS H Smith, S M Forrest, D C Williams, et al.
Annals of Neurology|May 13, 1999
Direct evidence that mitochondrial iron accumulation occurs in Friedreich ataxiaM B Delatycki, J Camakaris, H Brooks, et al.
Nucleic Acids Research|March 11, 1987
Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patientsT J Smith, L Wilson, S J Kenwrick, et al.
Genomics|November 1, 1988
Molecular and genetic mapping of the mouse mdx locusJ S Cavanna, G Coulton, J E Morgan, et al.
Familial Cancer|October 24, 2003
Profuse familial adenomatous polyposis with an adenomatous polyposis coli exon 3 mutationS Nasioulas, I T Jones, D J St John, et al.
Journal of Medical Genetics|February 1, 1996
Familial adenomatous polyposis in a 5 year old child: a clinical, pathological, and molecular genetic studyS Distante, S Nasioulas, G R Somers, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Nature|October 15, 1987
Preferential deletion of exons in Duchenne and Becker muscular dystrophiesS M Forrest, G S Cross, A Speer, et al.
Genomics|February 1, 1988
Further studies of gene deletions that cause Duchenne and Becker muscular dystrophiesS M Forrest, G S Cross, T Flint, et al.
Human Genetics|October 1, 1988
Patterns of exon deletions in Duchenne and Becker muscular dystrophyA P Read, R C Mountford, S M Forrest, et al.
British Medical Bulletin|July 1, 1989
Molecular analysis of Duchenne and Becker muscular dystrophiesD R Love, S M Forrest, T J Smith, et al.
Carbohydrate Research|June 26, 1992
Regioselectivity of the insertion reactions of some aromatic diazo compound complexes with cyclomaltoheptaoseS H Smith, S M Forrest, D C Williams, et al.
Annals of Neurology|May 13, 1999
Direct evidence that mitochondrial iron accumulation occurs in Friedreich ataxiaM B Delatycki, J Camakaris, H Brooks, et al.
Nucleic Acids Research|March 11, 1987
Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patientsT J Smith, L Wilson, S J Kenwrick, et al.
Genomics|November 1, 1988
Molecular and genetic mapping of the mouse mdx locusJ S Cavanna, G Coulton, J E Morgan, et al.
Familial Cancer|October 24, 2003
Profuse familial adenomatous polyposis with an adenomatous polyposis coli exon 3 mutationS Nasioulas, I T Jones, D J St John, et al.
Journal of Medical Genetics|February 1, 1996
Familial adenomatous polyposis in a 5 year old child: a clinical, pathological, and molecular genetic studyS Distante, S Nasioulas, G R Somers, et al.
Pageof 5