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Journal Abstract Search

225 related items for PubMed ID: 2563842

  • 21. DNA polymorphisms and deletion analysis of the Duchenne-Becker muscular dystrophy gene in the Chinese.
    Soong BW, Tsai TF, Su CH, Kao KP, Hsiao KJ, Su TS.
    Am J Med Genet; 1991 Mar 15; 38(4):593-600. PubMed ID: 1676564
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  • 27. The differential diagnosis of the human dystrophinopathies and related disorders.
    Kakulas BA.
    Curr Opin Neurol; 1996 Oct 15; 9(5):380-8. PubMed ID: 8894415
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  • 29. [Carrier detection in families affected by Duchenne/Becker muscular dystrophy].
    Pikó H, Nagy B, Balog J, Bán Z, Herczegfalvi A, Karcagi V.
    Orv Hetil; 2007 Dec 23; 148(51):2403-9. PubMed ID: 18055393
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  • 30. Manifesting carrier of Becker muscular dystrophy (BMD): clinical and recombinant DNA studies.
    Ionasescu VV, Searby CC, Ionasescu R.
    Acta Neurol Scand; 1989 Jun 23; 79(6):500-3. PubMed ID: 2782030
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  • 31. [Molecular pathology of Duchenne and Becker muscular dystrophy].
    Sugita H.
    Rinsho Shinkeigaku; 1990 Dec 23; 30(12):1309-16. PubMed ID: 2099874
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  • 32. DNA restriction fragment length polymorphisms in differential diagnosis of genetic disease: application in neuromuscular diseases.
    Defesche JC, de Vissar M, Bakker E, Bouwsma G, de Vijlder JJ, Bolhuis PA.
    Hum Genet; 1989 Apr 23; 82(1):55-8. PubMed ID: 2565867
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  • 38. The frequency of patients with dystrophin abnormalities in a limb-girdle patient population.
    Arikawa E, Hoffman EP, Kaido M, Nonaka I, Sugita H, Arahata K.
    Neurology; 1991 Sep 23; 41(9):1491-6. PubMed ID: 1842672
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  • 40. Prenatal diagnosis of Duchenne muscular dystrophy: prospective linkage analysis and retrospective dystrophin cDNA analysis.
    Ward PA, Hejtmancik JF, Witkowski JA, Baumbach LL, Gunnell S, Speer J, Hawley P, Tantravahi U, Caskey CT.
    Am J Hum Genet; 1989 Feb 23; 44(2):270-81. PubMed ID: 2643315
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