Author:
Dahl N.,Goonewardena P.,Chotai J.,Anvret M.,Pettersson U.
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference19 articles.
1. Ahrens P, Kruse TA (1986) An anonymous X-chromosomal clone identifying a frequent RFLP at Xp21-22. Nucleic Acids Res 14: 7819
2. Aldrigde J, Kunkel L, Bruns G, Tantravahi U, Lalande M, Brewster T, Moreau E, Wilson M, Bromley W, Roderick T, Latt SA (1984) A strategy to reveal high-frequency RFLPs along the human X-chromosome. Am J Hum Genet 36:546?564
3. Bakker E, Hofker MH, Goor N, Mandel JL, Wrogemann K, Davies K, Kunkel LM, Willard HF, Fenton WA, Sandkuyl L, Majoor-Krakauer D, Essen AJV, Jakoda MGJ, Sachs ES, Van Ommen GJB, Pearson PL (1985) Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closed linked RFLPs. Lancet 1:655?658
4. Brown CS, Thomas NST, Sarfarazi M, Davies KE, Kunkel L, Pearson PL, Kingston HM, Shaw DJ, Harper PS (1985) Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy. Hum Genet 71:62?74
5. Davies KE, Speer A, Herrmann F, Spiegler AW, McGlade S, Hofker MH, Briand P, Hanke R, Schwartz M, Steinbicker V, Szibor R, Korner H, Sommer D, Pearson PL, Contell C (1985) Human X chromosome markers and Duchenne muscular dystrophy. Nucleic Acids Res 13:3419?3426
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