Frame-Shift Deletions in Patients with Duchenne and Becker Muscular Dystrophy
Malhotra, S. B., Hart, K. A., Klamut, H. J., Thomas, N. S. T., Bodrug, S. E., Burghes, A. H. M., Bobrow, M., Harper, P. S., Thompson, M. W., Ray, P. N., Worton, R. G.
Published in Science (American Association for the Advancement of Science) (04.11.1988)
Published in Science (American Association for the Advancement of Science) (04.11.1988)
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Journal Article
Dystrophin in frameshift deletion patients with Becker muscular dystrophy
GANGOPADHYAY, S. B, SHERRATT, T. G, HECKMATT, J. Z, DUBOWITZ, V, MILLER, G, SHOKEIR, M, RAY, P. N, STRONG, P. N, WORTON, R. G
Published in American journal of human genetics (01.09.1992)
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Published in American journal of human genetics (01.09.1992)
Journal Article
Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3
Musarella, M.A., Weleber, R.G., Murphey, W.H., Young, R.S.L., Anson-Cartwright, L., Mets, M., Kraft, S.P., Polemeno, R., Litt, M., Worton, R.G.
Published in Genomics (San Diego, Calif.) (01.11.1989)
Published in Genomics (San Diego, Calif.) (01.11.1989)
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Journal Article
Molecular Analysis of a Constitutional X-Autosome Translocation in a Female with Muscular Dystrophy
Bodrug, S. E., Ray, P. N., Gonzalez, I. L., Schmickel, R. D., Sylvester, J. E., Worton, R. G.
Published in Science (American Association for the Advancement of Science) (25.09.1987)
Published in Science (American Association for the Advancement of Science) (25.09.1987)
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Journal Article
Gene therapy for duchenne muscular dystrophy — Early experiences with liposome-mediated gene transfer
Vitiello, L., Chonnt, A., Wasserman, J.D., Worton, R.G.
Published in Transfusion science (01.03.1996)
Published in Transfusion science (01.03.1996)
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Journal Article
Mapping of four translocation breakpoints within the Duchenne muscular dystrophy gene
Bodrug, S.E., Burghes, A.H.M., Ray, P.M., Worton, R.G.
Published in Genomics (San Diego, Calif.) (1989)
Published in Genomics (San Diego, Calif.) (1989)
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Journal Article
Linkage analysis of a large Latin-American family with X-linked retinitis pigmentosa and metallic sheen in the heterozygote carrier
Musarella, M.A., Anson-Cartwright, L., Burghes, A., Worton, R.G., Lesko, J.G., Nussbaum, R.L.
Published in Genomics (San Diego, Calif.) (01.05.1989)
Published in Genomics (San Diego, Calif.) (01.05.1989)
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