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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

133 related items for PubMed ID: 8329891

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  • 5. Variability in clinical, genetic and protein abnormalities in manifesting carriers of Duchenne and Becker muscular dystrophy.
    Bushby KM, Goodship JA, Nicholson LV, Johnson MA, Haggerty ID, Gardner-Medwin D.
    Neuromuscul Disord; 1993 Jan; 3(1):57-64. PubMed ID: 8329890
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  • 7. A homologue of dystrophin is expressed at the blood vessel membrane of DMD and BMD patients: immunological evidence.
    Augier N, Boucraut J, Léger J, Anoal M, Nicholson LV, Voelkel MA, Léger JJ, Pellissier JF.
    J Neurol Sci; 1992 Feb; 107(2):233-8. PubMed ID: 1564523
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  • 8. Molecular genetic and immunological analysis of dystrophin of a young patient with X-linked muscular dystrophy.
    Ikeya K, Saito K, Hayashi K, Tanaka H, Hagiwara Y, Yoshida M, Yamauchi A, Fukuyama Y, Ishiguro T, Eguchi C.
    Am J Med Genet; 1992 Jun 01; 43(3):580-7. PubMed ID: 1605252
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  • 12. Dystrophin in frameshift deletion patients with Becker muscular dystrophy.
    Gangopadhyay SB, Sherratt TG, Heckmatt JZ, Dubowitz V, Miller G, Shokeir M, Ray PN, Strong PN, Worton RG.
    Am J Hum Genet; 1992 Sep 01; 51(3):562-70. PubMed ID: 1496988
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  • 13. Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophies.
    Claustres M, Tuffery S, Chevron MP, Jozelon MP, Martinez P, Echenne B, Demaille J.
    Hum Genet; 1991 Dec 01; 88(2):179-84. PubMed ID: 1684565
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  • 16. Unusual expression and very mild course of Xp21 muscular dystrophy (Becker type) in a 60-year-old man with 26 percent deletion of the dystrophin gene.
    Palmucci L, Doriguzzi C, Mongini T, Restagno G, Chiadò-Piat L, Maniscalco M.
    Neurology; 1994 Mar 01; 44(3 Pt 1):541-3. PubMed ID: 8145928
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  • 18. [Muscular dystrophies detected by immunophenotyping and genotype analysis (mRNA and DNA)].
    Lukás Z, Vojtísková M, Fajkusová L, Bednarík J, Kadanka Z, Hájek J, Hermanová M, Vohánka S, Vytopil M.
    Cesk Patol; 2001 Nov 01; 37(4):137-45. PubMed ID: 11813630
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  • 19. Southern blot and PCR analyses of dystrophin gene deletions in Japanese patients with Duchenne muscular dystrophy.
    Nakajima T, Matsuo M, Nakamura H, Fujiwara Y.
    Kobe J Med Sci; 1991 Feb 01; 37(1):21-33. PubMed ID: 1921260
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  • 20. Dystrophin immunohistochemistry in a symptomatic carrier of Becker muscular dystrophy.
    Haginoya K, Yamamoto K, Iinuma K, Yanagisawa T, Ichinohasama Y, Shimmoto M, Suzuki Y, Tada K.
    J Neurol; 1991 Oct 01; 238(7):375-8. PubMed ID: 1683669
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