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Proceedings of the National Academy of Sciences of the United States of America|March 15, 1992
Point mutations in the dystrophin geneR G Roberts, M Bobrow, D R BentleyHuman Mutation|January 1, 1993
Infidelity in the structure of ectopic transcripts: a novel exon in lymphocyte dystrophin transcriptsR G Roberts, D R Bentley, M BobrowNucleic Acids Research|August 11, 1989
Detection of novel genetic markers by mismatch analysisR G Roberts, A J Montandon, M Bobrow, et al.Genomics|August 1, 1992
Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCRR G Roberts, A J Coffey, M Bobrow, et al.Genomics|May 1, 1993
Exon structure of the human dystrophin geneR G Roberts, A J Coffey, M Bobrow, et al.Genomics|August 1, 1990
Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy geneS Abbs, R G Roberts, C G Mathew, et al.American Journal of Human Genetics|August 1, 1991
Direct detection of dystrophin gene rearrangements by analysis of dystrophin mRNA in peripheral blood lymphocytesR G Roberts, T F Barby, E Manners, et al.Lancet (London, England)|December 22, 1990
Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNAR G Roberts, D R Bentley, T F Barby, et al.Human Molecular Genetics|May 16, 1998
Dystrophins in vertebrates and invertebratesR G Roberts, M BobrowAmerican Journal of Human Genetics|August 1, 1995
The identification of point mutations in Duchenne muscular dystrophy patients by using reverse-transcription PCR and the protein truncation testR J Gardner, M Bobrow, R G RobertsPageof 26