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Journal Abstract Search

162 related items for PubMed ID: 7668258

  • 1. 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; 57(2):329-36. PubMed ID: 7668258
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  • 3. Molecular analysis of X-autosome translocations in females with Duchenne muscular dystrophy.
    Bodrug SE, Holden JJ, Ray PN, Worton RG.
    EMBO J; 1991 Dec; 10(12):3931-9. PubMed ID: 1935912
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  • 5. 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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  • 6. Mapping of four translocation breakpoints within the Duchenne muscular dystrophy gene.
    Bodrug SE, Burghes AH, Ray PM, Worton RG.
    Genomics; 1989 Jan 25; 4(1):101-4. PubMed ID: 2914705
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  • 7. Duchenne muscular dystrophy in a female with a translocation involving Xp21.
    Nevin NC, Hughes AE, Calwell M, Lim JH.
    J Med Genet; 1986 Apr 25; 23(2):171-3. PubMed ID: 3712394
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  • 8. Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.
    Ray PN, Belfall B, Duff C, Logan C, Kean V, Thompson MW, Sylvester JE, Gorski JL, Schmickel RD, Worton RG.
    Nature; 1986 Apr 25; 318(6047):672-5. PubMed ID: 3001530
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  • 9. Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.
    Jacobs PA, Hunt PA, Mayer M, Bart RD.
    Am J Hum Genet; 1981 Jul 25; 33(4):513-8. PubMed ID: 7258185
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  • 10. Molecular heterogeneity of translocations associated with muscular dystrophy.
    Boyd Y, Munro E, Ray P, Worton R, Monaco T, Kunkel L, Craig I.
    Clin Genet; 1987 Apr 25; 31(4):265-72. PubMed ID: 3594934
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  • 11. 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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  • 12. The problem of Duchenne muscular dystrophy.
    Worton RG, Ray PN, Bodrug S, Burghes AH, Hu X, Thompson MW.
    Philos Trans R Soc Lond B Biol Sci; 1988 Jun 15; 319(1194):275-84. PubMed ID: 2900521
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  • 13. Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation.
    Willett-Brozick JE, Savul SA, Richey LE, Baysal BE.
    Hum Genet; 2001 Aug 15; 109(2):216-23. PubMed ID: 11511928
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  • 15. Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.
    Bodrug SE, Roberson JR, Weiss L, Ray PN, Worton RG, Van Dyke DL.
    J Med Genet; 1990 Jul 15; 27(7):426-32. PubMed ID: 2395160
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  • 16. Further evidence for Xp21 location of Duchenne muscular dystrophy (DMD) locus: X;9 translocation in a female with DMD.
    Emanuel BS, Zackai EH, Tucker SH.
    J Med Genet; 1983 Dec 15; 20(6):461-3. PubMed ID: 6655672
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  • 19. 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 15; 25(2):231-6. PubMed ID: 3777020
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  • 20. The second case of a t(17;22) in a family with neurofibromatosis type 1: sequence analysis of the breakpoint regions.
    Kehrer-Sawatzki H, Häussler J, Krone W, Bode H, Jenne DE, Mehnert KU, Tümmers U, Assum G.
    Hum Genet; 1997 Feb 15; 99(2):237-47. PubMed ID: 9048928
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