DNA analysis of Duchenne and Becker muscular dystrophy using pERT87 genomic probes and dystrophin cDNA probes
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical)
Link
http://www.nature.com/articles/jhg199122.pdf
Reference21 articles.
1. Akita, Y., Ohno, S., Goto, J., Nakano, I., Takatsu, M., Sugita, H. and Suzuki, K. 1987. Diagnosis of Duchenne and Becker muscular, dystrophies by DNA polymorphism.Jpn. J. Human Genet. 32: 71–82.
2. Asano, J., Tomatsu, S., Sukekawa, K., Yamaguchi, S., Ikedo, Y., Minami, R., Iida, M., Nishimura, M., Nakagawa, M., Ohshiro, M. and Orii, T. 1990. Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophy.Jpn. J. Human Genet. 35: 159–168.
3. Bakker, E., Goor, N., Wrogemann, K., Kunkel, L.M., Fenton, W.A., Majoor-Krakauer, D., Jahoda, M.G., Van Ommen, G.J.B., Hofker, M.H., Mandel, J.L., Davies, K.E., Willard, H.F., Sandkuyl, L., Essen, A.J.V., Sachs, E.S. and Pearson, P.L. 1985. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs.Lancet 1: 655–658.
4. Bertelson, C.J., Bartley, J.A., Monaco, A.P., Colletti-Feener, C., Fischbeck, K. and Kunkel, L.M. 1986. Localization of Xp21 meiotic exchange points in Duchenne muscular dystrophy families.J. Med. Genet. 23: 531–537.
5. Bullock, D.G., McSweeney, F.M., Whitehead, T.P. and Edwards, J.H. 1979. Serum creatine kinase activity and carrier status for Duchenne muscular dystrophy.Lancet 2: 1370.
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