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Journal Abstract Search

145 related items for PubMed ID: 3024018

  • 1. Long-range restriction map around the Duchenne muscular dystrophy gene.
    Burmeister M, Lehrach H.
    Nature; ; 324(6097):582-5. PubMed ID: 3024018
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  • 5. Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis.
    Kenwrick S, Patterson M, Speer A, Fischbeck K, Davies K.
    Cell; 1987 Jan 30; 48(2):351-7. PubMed ID: 3026644
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  • 6. Update on the molecular genetics of Duchenne muscular dystrophy.
    Siddique T, Bartlett R, Pericak-Vance M, Yamaoka L, Koh J, Chen J, Hung WY, Kandt R, Roses AD.
    Aust Paediatr J; 1988 Jan 30; 24 Suppl 1():9-14. PubMed ID: 3060079
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  • 8. The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome.
    Brockdorff N, Cross GS, Cavanna JS, Fisher EM, Lyon MF, Davies KE, Brown SD.
    Nature; 1988 Jan 30; 328(6126):166-8. PubMed ID: 3600793
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  • 10. Germline mosaicism and Duchenne muscular dystrophy mutations.
    Bakker E, Van Broeckhoven C, Bonten EJ, van de Vooren MJ, Veenema H, Van Hul W, Van Ommen GJ, Vandenberghe A, Pearson PL.
    Nature; 1988 Jan 30; 329(6139):554-6. PubMed ID: 2889144
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  • 13. Towards a complete linkage map of the human X chromosome.
    Davies KE, Williamson R.
    Horiz Biochem Biophys; 1986 Jan 30; 8():1-50. PubMed ID: 2875929
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  • 14. Duchenne muscular dystrophy. Collaboration and progress.
    Goodfellow PN.
    Nature; 1986 Jan 30; 322(6074):12-3. PubMed ID: 3724849
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  • 15. Deletion analysis of Duchenne muscular dystrophy.
    Erdem H, Ayter S, Ozgüç M, Topçu M, Topaloğlu H, Renda Y.
    Turk J Pediatr; 1993 Jan 30; 35(1):15-21. PubMed ID: 8236513
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  • 17. Mapping of 12 translocation breakpoints in the Xp21 region with respect to the locus for Duchenne muscular dystrophy.
    Boyd Y, Cockburn D, Holt S, Munro E, Van Ommen GJ, Gillard B, Affara N, Ferguson-Smith M, Craig I.
    Cytogenet Cell Genet; 1988 Jan 30; 48(1):28-34. PubMed ID: 3180845
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  • 20. Interrelationship between gene, its product and phenotype in Duchenne and Becker muscular dystrophy.
    Hausmanowa-Petrusewicz I, Zaremba J, Fidziańska A, Zimowski J, Bisko M, Badurska B, Fidziańska E, Lusakowska A, Borkowska J.
    Acta Neurobiol Exp (Wars); 1993 Jan 30; 53(1):297-303. PubMed ID: 8317263
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