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Journal Abstract Search

117 related items for PubMed ID: 3826553

  • 1. Clinical features in a girl with Duchenne muscular dystrophy with an X-autosome translocation; (X;4)(p21;q26).
    Kimura S, Mitsuda T, Misugi N, Saito F, Tonomura A, Sugita H.
    Brain Dev; 1986; 8(6):619-23. PubMed ID: 3826553
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  • 4. Duchenne muscular dystrophy in a female with a translocation involving Xp21.
    Nevin NC, Hughes AE, Calwell M, Lim JH.
    J Med Genet; 1986 Apr; 23(2):171-3. PubMed ID: 3712394
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  • 6. Duchenne muscular dystrophy in a girl with an (X;15) translocation.
    Ribeiro MC, Melaragno MI, Schmidt B, Brunoni D, Gabbai AA, Hackel C.
    Am J Med Genet; 1986 Oct; 25(2):231-6. PubMed ID: 3777020
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  • 8. Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophy.
    Bodrug SE, Ray PN, Gonzalez IL, Schmickel RD, Sylvester JE, Worton RG.
    Science; 1987 Sep 25; 237(4822):1620-4. PubMed ID: 3629260
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  • 9. Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus.
    Zatz M, Vianna-Morgante AM, Campos P, Diament AJ.
    J Med Genet; 1981 Dec 25; 18(6):442-7. PubMed ID: 7334502
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  • 11. Xp21/autosome translocations. Case report and risk for Duchenne muscular dystrophy.
    Holden JJ, Smith A, MacLeod PM, Masotti R, Duncan AM.
    Clin Genet; 1986 Jun 25; 29(6):516-22. PubMed ID: 3742857
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  • 12. Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome.
    Verellen-Dumoulin C, Freund M, De Meyer R, Laterre C, Frédéric J, Thompson MW, Markovic VD, Worton RG.
    Hum Genet; 1984 Jun 25; 67(1):115-9. PubMed ID: 6745920
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  • 18. Sequence analysis of the breakpoint regions of an X;5 translocation in a female with Duchenne muscular dystrophy.
    van Bakel I, Holt S, Craig I, Boyd Y.
    Am J Hum Genet; 1995 Aug 25; 57(2):329-36. PubMed ID: 7668258
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  • 20. Muscular dystrophy in girls with X;autosome translocations.
    Boyd Y, Buckle V, Holt S, Munro E, Hunter D, Craig I.
    J Med Genet; 1986 Dec 25; 23(6):484-90. PubMed ID: 3806636
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