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P N Ray

Showing results (91-100 of 110) with videos related to

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Neurogenetics|March 25, 2000
Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7C F Rochette, L C Surh, P N Ray, et al.
American Journal of Human Genetics|September 1, 1992
Dystrophin in frameshift deletion patients with Becker muscular dystrophyS B Gangopadhyay, T G Sherratt, J Z Heckmatt, et al.
Experimental Cell Research|January 1, 1991
Dystrophin is tightly associated with the sarcolemma of mammalian skeletal muscle fibersE E Zubrzycka-Gaarn, O F Hutter, G Karpati, et al.
Journal of Medical Genetics|October 1, 1996
X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindredJ J MacKenzie, J Fitzpatrick, P Babyn, et al.
Human Molecular Genetics|June 1, 1993
Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophyA V Winnard, C J Klein, D D Coovert, et al.
Science (New York, N.Y.)|January 1, 1988
Human ribosomal RNA genes: orientation of the tandem array and conservation of the 5' endR G Worton, J Sutherland, J E Sylvester, et al.
American Journal of Medical Genetics|November 15, 1992
Monozygotic twins concordant for late-onset probable Alzheimer disease with suspected Alzheimer disease in four sibsH Karlinsky, J M Berg, A Lennox, et al.
Nature|December 19, 1985
Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophyP N Ray, B Belfall, C Duff, et al.
Nature|June 2, 1988
The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscleE E Zubrzycka-Gaarn, D E Bulman, G Karpati, et al.
Ophthalmology|May 1, 1994
Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophyD A Sigesmund, R G Weleber, D A Pillers, et al.
Pageof 11

Showing results (91-100 of 110) with videos related to

Sort By:
Pageof 11
Neurogenetics|March 25, 2000
Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7C F Rochette, L C Surh, P N Ray, et al.
American Journal of Human Genetics|September 1, 1992
Dystrophin in frameshift deletion patients with Becker muscular dystrophyS B Gangopadhyay, T G Sherratt, J Z Heckmatt, et al.
Experimental Cell Research|January 1, 1991
Dystrophin is tightly associated with the sarcolemma of mammalian skeletal muscle fibersE E Zubrzycka-Gaarn, O F Hutter, G Karpati, et al.
Journal of Medical Genetics|October 1, 1996
X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindredJ J MacKenzie, J Fitzpatrick, P Babyn, et al.
Human Molecular Genetics|June 1, 1993
Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophyA V Winnard, C J Klein, D D Coovert, et al.
Science (New York, N.Y.)|January 1, 1988
Human ribosomal RNA genes: orientation of the tandem array and conservation of the 5' endR G Worton, J Sutherland, J E Sylvester, et al.
American Journal of Medical Genetics|November 15, 1992
Monozygotic twins concordant for late-onset probable Alzheimer disease with suspected Alzheimer disease in four sibsH Karlinsky, J M Berg, A Lennox, et al.
Nature|December 19, 1985
Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophyP N Ray, B Belfall, C Duff, et al.
Nature|June 2, 1988
The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscleE E Zubrzycka-Gaarn, D E Bulman, G Karpati, et al.
Ophthalmology|May 1, 1994
Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophyD A Sigesmund, R G Weleber, D A Pillers, et al.
Pageof 11