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S M Forrest

Showing results (41-50 of 48) with videos related to

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The Journal of Gene Medicine|March 28, 2001
Atomic force microscopy imaging of DNA-cationic liposome complexes optimised for gene transfection into neuronal cellsL A Wangerek, H H Dahl, T J Senden, et al.
American Journal of Medical Genetics|October 26, 1999
Clinical and genetic study of Friedreich ataxia in an Australian populationM B Delatycki, D B Paris, R J Gardner, et al.
Lancet (London, England)|December 5, 1987
Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophyS M Forrest, T J Smith, G S Cross, et al.
Neuroreport|April 20, 1999
Early-onset Alzheimer's disease caused by a novel mutation at codon 219 of the presenilin-1 geneM J Smith, R J Gardner, M A Knight, et al.
American Journal of Medical Genetics|September 1, 1990
Characterization of deletions in the dystrophin gene giving mild phenotypesD R Love, T J Flint, R F Marsden, et al.
Nature|January 11, 1990
Very mild muscular dystrophy associated with the deletion of 46% of dystrophinS B England, L V Nicholson, M A Johnson, et al.
Human Molecular Genetics|May 23, 1998
Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxicationE P Treacy, B R Akerman, L M Chow, et al.
Journal of Medical Genetics|September 3, 2004
Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3N M Solomon, S A Ross, T Morgan, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
The Journal of Gene Medicine|March 28, 2001
Atomic force microscopy imaging of DNA-cationic liposome complexes optimised for gene transfection into neuronal cellsL A Wangerek, H H Dahl, T J Senden, et al.
American Journal of Medical Genetics|October 26, 1999
Clinical and genetic study of Friedreich ataxia in an Australian populationM B Delatycki, D B Paris, R J Gardner, et al.
Lancet (London, England)|December 5, 1987
Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophyS M Forrest, T J Smith, G S Cross, et al.
Neuroreport|April 20, 1999
Early-onset Alzheimer's disease caused by a novel mutation at codon 219 of the presenilin-1 geneM J Smith, R J Gardner, M A Knight, et al.
American Journal of Medical Genetics|September 1, 1990
Characterization of deletions in the dystrophin gene giving mild phenotypesD R Love, T J Flint, R F Marsden, et al.
Nature|January 11, 1990
Very mild muscular dystrophy associated with the deletion of 46% of dystrophinS B England, L V Nicholson, M A Johnson, et al.
Human Molecular Genetics|May 23, 1998
Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxicationE P Treacy, B R Akerman, L M Chow, et al.
Journal of Medical Genetics|September 3, 2004
Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3N M Solomon, S A Ross, T Morgan, et al.
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