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Journal Abstract Search

117 related items for PubMed ID: 3826553

  • 21. An X:autosome translocation stabilizes truncated dystrophin: implications for lack of truncated dystrophins in Duchenne muscular dystrophy.
    Fidzianska A, Morrone A, Pegoraro E, Ryniewicz B, Ilnicka A, Zammarchi E, Hoffman EP.
    Neuropediatrics; 1995 Jun; 26(3):163-7. PubMed ID: 7477755
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  • 22. Common sequence motifs at the rearrangement sites of a constitutional X/autosome translocation and associated deletion.
    Giacalone JP, Francke U.
    Am J Hum Genet; 1992 Apr; 50(4):725-41. PubMed ID: 1347968
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  • 25. Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy.
    Kean VM, Macleod HL, Thompson MW, Ray PN, Verellen-Dumoulin C, Worton RG.
    J Med Genet; 1986 Dec; 23(6):491-3. PubMed ID: 2879921
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  • 26. [Duchenne muscular dystrophy in a female with an X-autosome translocation].
    Narazaki O, Hanai T, Ueki Y, Mitsudome A.
    Rinsho Shinkeigaku; 1985 Apr; 25(4):432-6. PubMed ID: 4017373
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  • 27. Prenatal evaluation of a de novo X;9 translocation.
    Feldman B, Kramer RL, Ebrahim SA, Wolff DJ, Evans MI.
    Am J Med Genet; 1999 Aug 27; 85(5):476-8. PubMed ID: 10405445
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  • 28. 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 27; 23(6):494-500. PubMed ID: 2879922
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  • 29. X;autosome translocations in females with Duchenne or Becker muscular dystrophy.
    Dubowitz V.
    Nature; 1986 Dec 27; 322(6076):291-2. PubMed ID: 3461282
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  • 30. Molecular analysis of X-autosome translocations in females with Duchenne muscular dystrophy.
    Bodrug SE, Holden JJ, Ray PN, Worton RG.
    EMBO J; 1991 Dec 27; 10(12):3931-9. PubMed ID: 1935912
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  • 33. 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 27; 27(6):537-41. PubMed ID: 559260
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  • 34. Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes.
    Worton RG, Duff C, Sylvester JE, Schmickel RD, Willard HF.
    Science; 1984 Jun 29; 224(4656):1447-9. PubMed ID: 6729462
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  • 35. Cytogenetic analysis and muscle differentiation in a girl with severe muscular dystrophy.
    Meola G, Scarpini E, Velicogna M, Scarlato G, Larizza L, Conti AF.
    J Neurol; 1986 Jun 29; 233(3):168-70. PubMed ID: 3723154
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  • 37. 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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  • 38. [Duchenne muscular dystrophy carrier presenting with mosaic X chromosome constitution and muscular symptoms--with analysis of the barr bodies in the muscle].
    Kinoshita M, Ikeda K, Yoshimura M, Saku A, Watanabe K.
    Rinsho Shinkeigaku; 1990 Jun 01; 30(6):643-6. PubMed ID: 2225660
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  • 39. In utero fetal muscle biopsy for the diagnosis of Duchenne muscular dystrophy in a female fetus "suddenly at risk".
    Evans MI, Farrell SA, Greb A, Ray P, Johnson MP, Hoffman EP.
    Am J Med Genet; 1993 May 15; 46(3):309-12. PubMed ID: 8488877
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  • 40. Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patients.
    Smith TJ, Wilson L, Kenwrick SJ, Forrest SM, Speer A, Coutelle C, Davies KE.
    Nucleic Acids Res; 1987 Mar 11; 15(5):2167-74. PubMed ID: 3562224
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