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Journal Abstract Search

157 related items for PubMed ID: 3629260

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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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  • 3. 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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  • 4. 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; 1981 Jul 25; 318(6047):672-5. PubMed ID: 3001530
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  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. A cDNA clone from the Duchenne/Becker muscular dystrophy gene.
    Burghes AH, Logan C, Hu X, Belfall B, Worton RG, Ray PN.
    Nature; 1986 Apr 25; 328(6129):434-7. PubMed ID: 3614347
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. 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 25; 20(6):461-3. PubMed ID: 6655672
    [Abstract] [Full Text] [Related]

  • 9. Mapping of 12 translocation breakpoints in the Xp21 region with respect to the locus for Duchenne muscular dystrophy.
    Boyd Y, Cockburn D, Holt S, Munro E, Van Ommen GJ, Gillard B, Affara N, Ferguson-Smith M, Craig I.
    Cytogenet Cell Genet; 1988 Dec 25; 48(1):28-34. PubMed ID: 3180845
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. 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 29; 31(4):265-72. PubMed ID: 3594934
    [Abstract] [Full Text] [Related]

  • 12. 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 29; 18(6):442-7. PubMed ID: 7334502
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  • 17. 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 Dec 29; 8(6):619-23. PubMed ID: 3826553
    [Abstract] [Full Text] [Related]

  • 18. 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
    [Abstract] [Full Text] [Related]

  • 19. Molecular analysis of X-autosome translocations in females with Duchenne muscular dystrophy.
    Bodrug SE, Holden JJ, Ray PN, Worton RG.
    EMBO J; 1991 Dec 15; 10(12):3931-9. PubMed ID: 1935912
    [Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]

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