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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.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.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.Investigative Ophthalmology & Visual Science|February 1, 1995
mdxCv3 mouse is a model for electroretinography of Duchenne/Becker muscular dystrophyD A Pillers, R G Weleber, W R Woodward, et al.American Journal of Human Genetics|August 1, 1991
Hunter disease (mucopolysaccharidosis type II) associated with unbalanced inactivation of the X chromosomes in a karyotypically normal girlJ T Clarke, W L Greer, P M Strasberg, et al.Medical Care|November 15, 2000
Structured implicit review: a new method for monitoring nursing care qualityM L Pearson, J L Lee, B L Chang, et al.Pageof 13