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Human Molecular Genetics|May 1, 1995
A novel dystrophin isoform is required for normal retinal electrophysiologyV N D'Souza, T M Nguyen, G E Morris, et al.Journal of Neuropathology and Experimental Neurology|March 1, 1990
Age-related conversion of dystrophin-negative to -positive fiber segments of skeletal but not cardiac muscle fibers in heterozygote mdx miceG Karpati, E E Zubrzycka-Gaarn, S Carpenter, et al.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.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.The Journal of Veterinary Medical Science|January 21, 2026
Outcome of medical treatments combined with tamsulosin for feline ureteral obstructionYu Furusawa, Takeshi Sogawa, Tomohide Kuramoto, et al.Optics Express|May 29, 2009
Microring-resonator-based add-drop filters in SiN: fabrication and analysisTymon Barwicz, Milos Popović, Peter Rakich, 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.Pageof 12