N Nesslinger|S Horrocks|P N Ray|P Strasberg|I M MacDonald - JoVE Visualize

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The American Journal of Pathology|July 1, 1989

Dystrophin is expressed in mdx skeletal muscle fibers after normal myoblast implantationG Karpati, Y Pouliot, E Zubrzycka-Gaarn, et al.

Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|November 25, 2000

Autosomal dominant Stargardt-like macular dystrophy segregating in a large Canadian familyP S Lagali, I M MacDonald, I B Griesinger, et al.

Journal of Medical Genetics|December 1, 1986

Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophyM W Thompson, P N Ray, B Belfall, et al.

Biochimica Et Biophysica Acta|June 27, 1986

Regulation of renal sulfoglycolipid biosynthesisC A Lingwood, J Dennis, E Hsu, et al.

American Journal of Human Genetics|May 1, 1992

Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibersC J Klein, D D Coovert, D E Bulman, et al.

Journal of Medical Genetics|December 1, 1986

Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophyV M Kean, H L Macleod, M W Thompson, et al.

Journal of Medical Genetics|June 1, 1988

Partial gene duplication in Duchenne and Becker muscular dystrophiesX Y Hu, A H Burghes, P N Ray, et al.

Science (New York, N.Y.)|September 25, 1987

Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophyS E Bodrug, P N Ray, I L Gonzalez, et al.

Journal of Medical Genetics|July 1, 1990

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophyS E Bodrug, J R Roberson, L Weiss, et al.

Ophthalmic Paediatrics and Genetics|August 1, 1984

Corneal pathology and aniridia associated with partial trisomy 2q, due to a maternal (2;6) translocationI M MacDonald, W N Clarke, B G Clifford, et al.

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Showing results (91-100 of 137) with videos related to

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Pageof 14

The American Journal of Pathology|July 1, 1989

Dystrophin is expressed in mdx skeletal muscle fibers after normal myoblast implantationG Karpati, Y Pouliot, E Zubrzycka-Gaarn, et al.

Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|November 25, 2000

Autosomal dominant Stargardt-like macular dystrophy segregating in a large Canadian familyP S Lagali, I M MacDonald, I B Griesinger, et al.

Journal of Medical Genetics|December 1, 1986

Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophyM W Thompson, P N Ray, B Belfall, et al.

Biochimica Et Biophysica Acta|June 27, 1986

Regulation of renal sulfoglycolipid biosynthesisC A Lingwood, J Dennis, E Hsu, et al.

American Journal of Human Genetics|May 1, 1992

Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibersC J Klein, D D Coovert, D E Bulman, et al.

Journal of Medical Genetics|December 1, 1986

Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophyV M Kean, H L Macleod, M W Thompson, et al.

Journal of Medical Genetics|June 1, 1988

Partial gene duplication in Duchenne and Becker muscular dystrophiesX Y Hu, A H Burghes, P N Ray, et al.

Science (New York, N.Y.)|September 25, 1987

Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophyS E Bodrug, P N Ray, I L Gonzalez, et al.

Journal of Medical Genetics|July 1, 1990

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophyS E Bodrug, J R Roberson, L Weiss, et al.

Ophthalmic Paediatrics and Genetics|August 1, 1984

Corneal pathology and aniridia associated with partial trisomy 2q, due to a maternal (2;6) translocationI M MacDonald, W N Clarke, B G Clifford, et al.

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