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American Journal of Medical Genetics|February 5, 1998
Monozygotic twins with 45,X/46,XY mosaicism discordant for phenotypic sexT Costa, M Lambert, I Teshima, et al.American Journal of Medical Genetics|February 1, 1988
A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndromeS Wood, R J Shukin, B C McGillivray, et al.Neuromuscular Disorders : NMD|March 29, 2000
Expression and synthesis of alternatively spliced variants of Dp71 in adult human brainR C Austin, G E Morris, P L Howard, et al.American Journal of Human Genetics|April 1, 1990
Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotypegenotype correlationX Y Hu, P N Ray, E G Murphy, et al.Gene|August 1, 1989
Fine structure analysis of the Chinese hamster AS gene encoding asparagine synthetaseI L Andrulis, M Shotwell, S Evans-Blackler, et al.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.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.Pageof 12