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Journal Abstract Search

279 related items for PubMed ID: 8411068

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  • 2. Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 3. Differential diagnosis and prognosis.
    Nicholson LV, Johnson MA, Bushby KM, Gardner-Medwin D, Curtis A, Ginjaar IB, den Dunnen JT, Welch JL, Butler TJ, Bakker E.
    J Med Genet; 1993 Sep; 30(9):745-51. PubMed ID: 8411069
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  • 3. Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 1. Trends across the clinical groups.
    Nicholson LV, Johnson MA, Bushby KM, Gardner-Medwin D, Curtis A, Ginjaar IB, den Dunnen JT, Welch JL, Butler TJ, Bakker E.
    J Med Genet; 1993 Sep; 30(9):728-36. PubMed ID: 8411067
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  • 11. Deletion status and intellectual impairment in Duchenne muscular dystrophy.
    Bushby KM, Appleton R, Anderson LV, Welch JL, Kelly P, Gardner-Medwin D.
    Dev Med Child Neurol; 1995 Mar; 37(3):260-9. PubMed ID: 7890131
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  • 17. [Molecular genetics and problems found in genetic diagnosis of Duchenne Becker muscular dystrophy].
    Takeshima Y, Matsuo M.
    Nihon Rinsho; 1997 Dec; 55(12):3120-5. PubMed ID: 9436421
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  • 20. Frameshift deletions of exons 3-7 and revertant fibers in Duchenne muscular dystrophy: mechanisms of dystrophin production.
    Winnard AV, Mendell JR, Prior TW, Florence J, Burghes AH.
    Am J Hum Genet; 1995 Jan; 56(1):158-66. PubMed ID: 7825572
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