R G Fenwick - JoVE Visualize

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Science (New York, N.Y.)|May 18, 1992

Triplet repeat mutations in human diseaseC T Caskey, A Pizzuti, Y H Fu, et al.

Human Mutation|January 1, 1994

A robotics-assisted procedure for large scale cystic fibrosis mutation analysisJ M DeMarchi, C S Richards, R G Fenwick, et al.

JAMA|April 21, 1993

Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspringJ B Redman, R G Fenwick, Y H Fu, et al.

American Journal of Medical Genetics|September 1, 1991

Discordance of muscular dystrophy in monozygotic female twins: evidence supporting asymmetric splitting of the inner cell mass in a manifesting carrier of Duchenne dystrophyJ R Lupski, C A Garcia, H Y Zoghbi, et al.

Neurology|September 1, 1992

Premature chain termination mutation causing Duchenne muscular dystrophyP R Clemens, P A Ward, C T Caskey, et al.

Cell|October 1, 1977

Forward and reverse mutations affecting the kinetics and apparent molecular weight of mammalian HGPRTR G Fenwick, T H Sawyer, G D Kruh, et al.

Genomics|June 1, 1994

Linkage disequilibria among (CA)n polymorphisms in the human dystrophin gene and their implications in carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophiesR Chakraborty, Y Zhong, M de Andrade, et al.

The Journal of Cell Biology|September 1, 1989

The apolipoprotein A-I gene is actively expressed in the rapidly myelinating avian peripheral nerveA C LeBlanc, M Földvári, D F Spencer, et al.

Plasmid|March 1, 1986

Characterization of transferable plasmids from Shigella flexneri 2a that confer resistance to trimethoprim, streptomycin, and sulfonamidesA C Chinault, V A Blakesley, E Roessler, et al.

American Journal of Human Genetics|November 1, 1991

Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphismsP R Clemens, R G Fenwick, J S Chamberlain, et al.

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Showing results (21-30 of 37) with videos related to

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Pageof 4

Science (New York, N.Y.)|May 18, 1992

Triplet repeat mutations in human diseaseC T Caskey, A Pizzuti, Y H Fu, et al.

Human Mutation|January 1, 1994

A robotics-assisted procedure for large scale cystic fibrosis mutation analysisJ M DeMarchi, C S Richards, R G Fenwick, et al.

JAMA|April 21, 1993

Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspringJ B Redman, R G Fenwick, Y H Fu, et al.

American Journal of Medical Genetics|September 1, 1991

Discordance of muscular dystrophy in monozygotic female twins: evidence supporting asymmetric splitting of the inner cell mass in a manifesting carrier of Duchenne dystrophyJ R Lupski, C A Garcia, H Y Zoghbi, et al.

Neurology|September 1, 1992

Premature chain termination mutation causing Duchenne muscular dystrophyP R Clemens, P A Ward, C T Caskey, et al.

Cell|October 1, 1977

Forward and reverse mutations affecting the kinetics and apparent molecular weight of mammalian HGPRTR G Fenwick, T H Sawyer, G D Kruh, et al.

Genomics|June 1, 1994

Linkage disequilibria among (CA)n polymorphisms in the human dystrophin gene and their implications in carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophiesR Chakraborty, Y Zhong, M de Andrade, et al.

The Journal of Cell Biology|September 1, 1989

The apolipoprotein A-I gene is actively expressed in the rapidly myelinating avian peripheral nerveA C LeBlanc, M Földvári, D F Spencer, et al.

Plasmid|March 1, 1986

Characterization of transferable plasmids from Shigella flexneri 2a that confer resistance to trimethoprim, streptomycin, and sulfonamidesA C Chinault, V A Blakesley, E Roessler, et al.

American Journal of Human Genetics|November 1, 1991

Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphismsP R Clemens, R G Fenwick, J S Chamberlain, et al.

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