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British Medical Bulletin|July 1, 1989
Myogenic regulation of dystrophin gene expressionH J Klamut, E E Zubrzycka-Gaarn, D E Bulman, et al.Cytogenetic and Genome Research|April 1, 2006
New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndromeA C Smith, T Rubin, C Shuman, et al.Neurogenetics|June 5, 2013
Autosomal recessive hereditary spastic paraplegia-clinical and genetic characteristics of a well-defined cohortG Yoon, B Baskin, M Tarnopolsky, et al.Gene|November 14, 1998
Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin geneJ C McNaughton, D J Cockburn, G Hughes, et al.American Journal of Human Genetics|June 1, 1997
Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy numberP E McAndrew, D W Parsons, L R Simard, et al.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.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.Pageof 14