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Journal Abstract Search

133 related items for PubMed ID: 8329891

  • 21. Direct carrier detection by in situ suppression hybridization with cosmid clones of the Duchenne/Becker muscular dystrophy locus.
    Ried T, Mahler V, Vogt P, Blonden L, van Ommen GJ, Cremer T, Cremer M.
    Hum Genet; 1990 Oct; 85(6):581-6. PubMed ID: 2227948
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  • 22. Phenotypic Duchenne muscular dystrophy with C-terminal domain.
    Higuchi I, Fukunaga H, Usuki F, Moritoyo T, Osame M.
    Pediatr Neurol; 1992 Oct; 8(4):310-2. PubMed ID: 1388424
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  • 23. The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. II. Correlation of phenotype with genetic and protein abnormalities.
    Bushby KM, Gardner-Medwin D, Nicholson LV, Johnson MA, Haggerty ID, Cleghorn NJ, Harris JB, Bhattacharya SS.
    J Neurol; 1993 Feb; 240(2):105-12. PubMed ID: 8437017
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  • 24. Is dystrophin labelling always discontinuous in Becker muscular dystrophy?
    Slater CR, Nicholson LV.
    J Neurol Sci; 1991 Feb; 101(2):187-92. PubMed ID: 2033404
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  • 25. Asymptomatic Becker muscular dystrophy: expression of dystrophin and dystrophin-related protein.
    Tachi N, Wakai S, Watanabe Y, Ohya K, Chiba S.
    Pediatr Neurol; 1993 Feb; 9(3):207-9. PubMed ID: 8352853
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  • 26. A case of myopathy associated with a dystrophin gene deletion and abnormal glycogen storage.
    Rose MR, Howard RS, Genet SA, McMahon CJ, Whitfield A, Morgan-Hughes JA.
    Muscle Nerve; 1993 Jan; 16(1):57-62. PubMed ID: 8423832
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  • 27. Prediction of dystrophin phenotype by DNA analysis in Duchenne/Becker muscular dystrophy.
    Specht LA, Beggs AH, Korf B, Kunkel LM, Shapiro F.
    Pediatr Neurol; 1992 Jan; 8(6):432-6. PubMed ID: 1476571
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  • 28. Multiplicity of abnormal dystrophin in Becker muscular dystrophy. A Becker muscular dystrophy gene frequently produced two smaller sizes of dystrophin.
    Hori S, Ohtani S, Shimizu T, Ibi T, Sahashi K, Nonaka I, Miyamoto K, Tanabe H.
    J Neurol Sci; 1994 Feb; 121(2):183-9. PubMed ID: 8158213
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  • 30. Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlates.
    Comi GP, Prelle A, Bresolin N, Moggio M, Bardoni A, Gallanti A, Vita G, Toscano A, Ferro MT, Bordoni A.
    Brain; 1994 Feb; 117 ( Pt 1)():1-14. PubMed ID: 8149204
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  • 31. Delayed expression of dystrophin on regenerating muscle from two siblings with Becker muscular dystrophy.
    Tachi N, Wakai S, Watanabe Y, Chiba S, Nagaoka M, Minami R.
    J Neurol Sci; 1992 Jul; 110(1-2):165-8. PubMed ID: 1506856
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  • 32. Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapy.
    Passos-Bueno MR, Vainzof M, Marie SK, Zatz M.
    Hum Mol Genet; 1994 Jun; 3(6):919-22. PubMed ID: 7951237
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  • 33. Identification of a mutation in the promoter region of the dystrophin gene in a patient with atypical Becker muscular dystrophy.
    Bushby KM, Cleghorn NJ, Curtis A, Haggerty ID, Nicholson LV, Johnson MA, Harris JB, Bhattacharya SS.
    Hum Genet; 1991 Dec; 88(2):195-9. PubMed ID: 1757094
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  • 34. Additional dystrophin fragment in Becker muscular dystrophy may result from proteolytic cleavage at deletion junctions.
    Beggs AH, Hoffman EP, Kunkel LM.
    Am J Med Genet; 1992 Oct 01; 44(3):378-81. PubMed ID: 1488990
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