Showing results (71-80 of 137) with videos related to
Sort By:
Pageof 14
Human Molecular Genetics|September 1, 1995
Cloning and characterization of alternatively spliced isoforms of Dp71R C Austin, P L Howard, V N D'Souza, et al.Nature|July 5, 1987
A cDNA clone from the Duchenne/Becker muscular dystrophy geneA H Burghes, C Logan, X Hu, et al.Genomics|June 1, 1991
Point mutation in the human dystrophin gene: identification through western blot analysisD E Bulman, S B Gangopadhyay, K G Bebchuck, et al.American Journal of Human Genetics|June 1, 1989
Evidence for mutation by unequal sister chromatid exchange in the Duchenne muscular dystrophy geneX Y Hu, A H Burghes, D E Bulman, et al.The British Journal of Dermatology|August 3, 2006
Preferences for aspects of a dermatology consultationJ Coast, C Salisbury, D de Berker, et al.American Journal of Medical Genetics|March 29, 1996
FISH detection of chromosome 15 deletions in Prader-Willi and Angelman syndromesI Teshima, D Chadwick, D Chitayat, et al.Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|February 1, 1987
Norrie's disease in a French-Canadian kindred: attempt to detect carriers by DNA analysisR C Polomeno, S Zeesman, I M MacDonald, et al.Muscle & Nerve|May 1, 1990
Dystrophin is localized to the plasma membrane of human skeletal muscle fibers by electron-microscopic cytochemical studyS Carpenter, G Karpati, E Zubrzycka-Gaarn, et al.American Journal of Human Genetics|February 1, 1991
Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific for dystrophinD E Bulman, E G Murphy, E E Zubrzycka-Gaarn, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|June 15, 1988
The problem of Duchenne muscular dystrophyR G Worton, P N Ray, S Bodrug, et al.Pageof 14