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Journal Abstract Search

154 related items for PubMed ID: 2885783

  • 1. 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; 37(7):1147-51. PubMed ID: 2885783
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  • 3. 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. 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 01; 27(6):537-41. PubMed ID: 559260
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  • 5. 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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  • 8. Duchenne muscular dystrophy in one of monozygotic twin girls.
    Burn J, Povey S, Boyd Y, Munro EA, West L, Harper K, Thomas D.
    J Med Genet; 1986 Dec 15; 23(6):494-500. PubMed ID: 2879922
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  • 9. Becker muscular dystrophy recombinant DNA studies in identical twins.
    Ionasescu V, Ionasescu R, Searby C, Burns T.
    Muscle Nerve; 1988 Apr 15; 11(4):287-90. PubMed ID: 3398874
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  • 12. [Carrier detection and gene analysis in a Duchenne muscular dystrophy family].
    Lu FM.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1990 Aug 15; 23(4):231-3, 255. PubMed ID: 1979269
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  • 13. A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome.
    Wood S, Shukin RJ, McGillivray BC, Ray PN, Worton RG.
    Am J Med Genet; 1988 Feb 15; 29(2):419-23. PubMed ID: 2895584
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  • 19. Prenatal diagnosis and carrier detection by DNA studies in a Duchenne muscular dystrophy family with no living affected male.
    Chen JD, Denton MJ, Serravalle S, Morgan G.
    Aust Paediatr J; 1988 Dec 15; 24(6):351-3. PubMed ID: 2907402
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