R G Fenwick - JoVE Visualize

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Neurology|September 1, 1991

9p monosomy in a patient with Gilles de la Tourette's syndromeL D Taylor, D B Krizman, J Jankovic, et al.

American Journal of Human Genetics|March 1, 1994

Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophyT Ashizawa, M Anvret, M Baiget, et al.

American Journal of Medical Genetics|July 15, 1994

Asymmetry of methylation with FMR-1 full mutation in two 45,X/46,XX mosaic females associated with normal intellectL R Shapiro, R J Simensen, P L Wilmot, et al.

Science (New York, N.Y.)|March 16, 1992

An unstable triplet repeat in a gene related to myotonic muscular dystrophyY H Fu, A Pizzuti, R G Fenwick, et al.

Science (New York, N.Y.)|April 9, 1993

Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophyY H Fu, D L Friedman, S Richards, et al.

Cell|December 30, 1991

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradoxY H Fu, D P Kuhl, A Pizzuti, et al.

JAMA|May 20, 1992

Diagnosis of Duchenne and Becker muscular dystrophies by polymerase chain reaction. A multicenter studyJ S Chamberlain, J R Chamberlain, R G Fenwick, et al.

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Showing results (31-40 of 37) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 37 results.

Neurology|September 1, 1991

9p monosomy in a patient with Gilles de la Tourette's syndromeL D Taylor, D B Krizman, J Jankovic, et al.

American Journal of Human Genetics|March 1, 1994

Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophyT Ashizawa, M Anvret, M Baiget, et al.

American Journal of Medical Genetics|July 15, 1994

Asymmetry of methylation with FMR-1 full mutation in two 45,X/46,XX mosaic females associated with normal intellectL R Shapiro, R J Simensen, P L Wilmot, et al.

Science (New York, N.Y.)|March 16, 1992

An unstable triplet repeat in a gene related to myotonic muscular dystrophyY H Fu, A Pizzuti, R G Fenwick, et al.

Science (New York, N.Y.)|April 9, 1993

Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophyY H Fu, D L Friedman, S Richards, et al.

Cell|December 30, 1991

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradoxY H Fu, D P Kuhl, A Pizzuti, et al.

JAMA|May 20, 1992

Diagnosis of Duchenne and Becker muscular dystrophies by polymerase chain reaction. A multicenter studyJ S Chamberlain, J R Chamberlain, R G Fenwick, et al.

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