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Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
Kunkel LM, Hejtmancik JF, Caskey CT, Speer A, Monaco AP, Middlesworth W, Colletti CA, Bertelson C, Müller U, Bresnan M, Shapiro F, Tantravahi U, Speer J, Latt SA, Bartlett R, Pericak-Vance MA, Roses AD, Thompson MW, Ray PN, Worton RG, Fischbeck KH, Gallano P, Coulon M, Duros C, Boue J, Junien C, Chelly J, Hamard G, Jeanpierre M, Lambert M, Kaplan JC, Emery A, Dorkins H, McGlade S, Davies KE, Boehm C, Arveiler B, Lemaire C, Morgan GJ, Denton MJ, Amos J, Bobrow M, Benham F, Boswinkel E, Cole C, Dubowitz V, Hart K, Hodgson S, Johnson L, Walker A, Roncuzzi L, Ferlini A, Nobile C, Romeo G, Wilcox DE, Affara NA, Ferguson-Smith MA, Lindolf M, Kaariainen H, de la Chapelle A, Ionasescu V, Searby C, Ionasescu R, Bakker E, van Ommen GJ, Pearson PL, Greenberg CR, Hamerton JL, Wrogemann K, Doherty RA, Polakowska R, Hyser C, Quirk S, Thomas N, Harper JF, Darras BT, Francke U. Kunkel LM, et al. Among authors: speer j, speer a. Nature. 1986 Jul 3-9;322(6074):73-7. doi: 10.1038/322073a0. Nature. 1986. PMID: 3014348
Molecular analysis of Duchenne and Becker muscular dystrophies.
Love DR, Forrest SM, Smith TJ, England S, Flint T, Davies KE, Speer A. Love DR, et al. Among authors: speer a. Br Med Bull. 1989 Jul;45(3):659-80. doi: 10.1093/oxfordjournals.bmb.a072351. Br Med Bull. 1989. PMID: 2688822 Review.
Human X chromosome markers and Duchenne muscular dystrophy.
Davies KE, Speer A, Herrmann F, Spiegler AW, McGlade S, Hofker MH, Briand P, Hanke R, Schwartz M, Steinbicker V, et al. Davies KE, et al. Among authors: speer a. Nucleic Acids Res. 1985 May 24;13(10):3419-26. doi: 10.1093/nar/13.10.3419. Nucleic Acids Res. 1985. PMID: 3859837 Free PMC article.
220 results