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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

240 related items for 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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  • 7. Uniparental disomy of the entire X chromosome in a female with Duchenne muscular dystrophy.
    Quan F, Janas J, Toth-Fejel S, Johnson DB, Wolford JK, Popovich BW.
    Am J Hum Genet; 1997 Jan 15; 60(1):160-5. PubMed ID: 8981959
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  • 10. Failure of inactivation of Duchenne dystrophy X-chromosome in one of female identical twins.
    Gomez MR, Engel AG, Dewald G, Peterson HA.
    Neurology; 1977 Jun 15; 27(6):537-41. PubMed ID: 559260
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  • 11. X inactivation and dystrophin studies in a t(X;12) female: evidence for biochemical normalization in Duchenne muscular dystrophy carriers.
    Wenger SL, Steele MW, Hoffman EP, Barmada MA, Wessel HB.
    Am J Med Genet; 1992 Aug 01; 43(6):1012-5. PubMed ID: 1415326
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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 01; 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 01; 32(2):268-73. PubMed ID: 2648829
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