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Journal Abstract Search

240 related items for PubMed ID: 2180286

  • 1. Skewed X inactivation in a female MZ twin results in Duchenne muscular dystrophy.
    Richards CS, Watkins SC, Hoffman EP, Schneider NR, Milsark IW, Katz KS, Cook JD, Kunkel LM, Cortada JM.
    Am J Hum Genet; 1990 Apr; 46(4):672-81. PubMed ID: 2180286
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  • 2. Discordance of muscular dystrophy in monozygotic female twins: evidence supporting asymmetric splitting of the inner cell mass in a manifesting carrier of Duchenne dystrophy.
    Lupski JR, Garcia CA, Zoghbi HY, Hoffman EP, Fenwick RG.
    Am J Med Genet; 1991 Sep 01; 40(3):354-64. PubMed ID: 1683155
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  • 4. Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X-chromosome inactivation.
    Abbadi N, Philippe C, Chery M, Gilgenkrantz H, Tome F, Collin H, Theau D, Recan D, Broux O, Fardeau M.
    Am J Med Genet; 1994 Aug 15; 52(2):198-206. PubMed ID: 7802009
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  • 9. Monozygotic female twin carriers discordant for the clinical manifestations of Duchenne muscular dystrophy.
    Chutkow JG, Hyser CL, Edwards JA, Heffner RR, Czyrny JJ.
    Neurology; 1987 Jul 15; 37(7):1147-51. PubMed ID: 2885783
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  • 12. Brother/sister pairs affected with early-onset, progressive muscular dystrophy: molecular studies reveal etiologic heterogeneity.
    Francke U, Darras BT, Hersh JH, Berg BO, Miller RG.
    Am J Hum Genet; 1989 Jul 15; 45(1):63-72. PubMed ID: 2568091
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  • 14. X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.
    Towbin JA, Hejtmancik JF, Brink P, Gelb B, Zhu XM, Chamberlain JS, McCabe ER, Swift M.
    Circulation; 1993 Jun 15; 87(6):1854-65. PubMed ID: 8504498
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  • 18. Dystrophin immunocytochemistry in muscle culture: detection of a carrier of Duchenne muscular dystrophy.
    Miranda AF, Francke U, Bonilla E, Martucci G, Schmidt B, Salviati G, Rubin M.
    Am J Med Genet; 1989 Feb 15; 32(2):268-73. PubMed ID: 2648829
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