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Journal Abstract Search

195 related items for PubMed ID: 1496988

  • 1. 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; 51(3):562-70. PubMed ID: 1496988
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  • 2. Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophy.
    Winnard AV, Klein CJ, Coovert DD, Prior T, Papp A, Snyder P, Bulman DE, Ray PN, McAndrew P, King W.
    Hum Mol Genet; 1993 Jun; 2(6):737-44. PubMed ID: 8353493
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  • 3. 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; 88(2):179-84. PubMed ID: 1684565
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  • 4. Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy.
    Malhotra SB, Hart KA, Klamut HJ, Thomas NS, Bodrug SE, Burghes AH, Bobrow M, Harper PS, Thompson MW, Ray PN.
    Science; 1988 Nov 04; 242(4879):755-9. PubMed ID: 3055295
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  • 5. Exon skipping and translation in patients with frameshift deletions in the dystrophin gene.
    Sherratt TG, Vulliamy T, Dubowitz V, Sewry CA, Strong PN.
    Am J Hum Genet; 1993 Nov 04; 53(5):1007-15. PubMed ID: 8213828
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  • 6. A novel splice site mutation in a Becker muscular dystrophy patient.
    Bartolo C, Papp AC, Snyder PJ, Sedra MS, Burghes AH, Hall CD, Mendell JR, Prior TW.
    J Med Genet; 1996 Apr 04; 33(4):324-7. PubMed ID: 8730289
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  • 9. Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies.
    Chelly J, Gilgenkrantz H, Lambert M, Hamard G, Chafey P, Récan D, Katz P, de la Chapelle A, Koenig M, Ginjaar IB.
    Cell; 1990 Dec 21; 63(6):1239-48. PubMed ID: 2261642
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  • 11. Deletions in the dystrophin gene: analysis of Duchenne and Becker muscular dystrophy patients in Quebec.
    Simard LR, Gingras F, Delvoye N, Vanasse M, Melançon SB, Labuda D.
    Hum Genet; 1992 Jun 21; 89(4):419-24. PubMed ID: 1618490
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  • 12. Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients.
    Dinçer P, Topaloğlu H, Ayter S, Ozgüç M, Taşdemir HA, Renda Y.
    Brain Dev; 1996 Jun 21; 18(2):91-4. PubMed ID: 8733896
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  • 15. Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 2. Correlations within individual patients.
    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 21; 30(9):737-44. PubMed ID: 8411068
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  • 16. The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.
    Koenig M, Beggs AH, Moyer M, Scherpf S, Heindrich K, Bettecken T, Meng G, Müller CR, Lindlöf M, Kaariainen H, de la Chapellet A, Kiuru A, Savontaus ML, Gilgenkrantz H, Récan D, Chelly J, Kaplan JC, Covone AE, Archidiacono N, Romeo G, Liechti-Gailati S, Schneider V, Braga S, Moser H, Darras BT, Murphy P, Francke U, Chen JD, Morgan G, Denton M, Greenberg CR, Wrogemann K, Blonden LA, van Paassen MB, van Ommen GJ, Kunkel LM.
    Am J Hum Genet; 1989 Oct 21; 45(4):498-506. PubMed ID: 2491009
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  • 19. Frameshift deletion mechanisms in Egyptian Duchenne and Becker muscular dystrophy families.
    Elhawary NA, Shawky RM, Hashem N.
    Mol Cells; 2004 Oct 31; 18(2):141-9. PubMed ID: 15528988
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  • 20. [Molecular genetics and problems found in genetic diagnosis of Duchenne Becker muscular dystrophy].
    Takeshima Y, Matsuo M.
    Nihon Rinsho; 1997 Dec 31; 55(12):3120-5. PubMed ID: 9436421
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