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109 related items for PubMed ID: 3243546

  • 1. Mapping of Xp21 translocation breakpoints in and around the DMD gene by pulsed field gel electrophoresis.
    Meitinger T, Boyd Y, Anand R, Craig IW.
    Genomics; 1988 Nov; 3(4):315-22. PubMed ID: 3243546
    [Abstract] [Full Text] [Related]

  • 2. 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 Nov; 48(1):28-34. PubMed ID: 3180845
    [Abstract] [Full Text] [Related]

  • 3. Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis.
    Kenwrick S, Patterson M, Speer A, Fischbeck K, Davies K.
    Cell; 1987 Jan 30; 48(2):351-7. PubMed ID: 3026644
    [Abstract] [Full Text] [Related]

  • 4. 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 30; 18(6):442-7. PubMed ID: 7334502
    [Abstract] [Full Text] [Related]

  • 5. Mapping of four translocation breakpoints within the Duchenne muscular dystrophy gene.
    Bodrug SE, Burghes AH, Ray PM, Worton RG.
    Genomics; 1989 Jan 30; 4(1):101-4. PubMed ID: 2914705
    [Abstract] [Full Text] [Related]

  • 6. 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 30; 33(4):513-8. PubMed ID: 7258185
    [Abstract] [Full Text] [Related]

  • 7. Long-range genomic map of the Duchenne muscular dystrophy (DMD) gene: isolation and use of J66 (DXS268), a distal intragenic marker.
    van Ommen GJ, Bertelson C, Ginjaar HB, den Dunnen JT, Bakker E, Chelly J, Matton M, van Essen AJ, Bartley J, Kunkel LM.
    Genomics; 1987 Dec 30; 1(4):329-36. PubMed ID: 2896627
    [Abstract] [Full Text] [Related]

  • 8. 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 30; 23(6):484-90. PubMed ID: 3806636
    [Abstract] [Full Text] [Related]

  • 9. 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 30; 57(2):329-36. PubMed ID: 7668258
    [Abstract] [Full Text] [Related]

  • 10. 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 30; 20(6):461-3. PubMed ID: 6655672
    [Abstract] [Full Text] [Related]

  • 11. Localization of DNA sequences to a region within Xp11.21 between incontinentia pigmenti (IP1) X-chromosomal translocation breakpoints.
    Gorski JL, Burright EN, Harnden CE, Stein CK, Glover TW, Reyner EL.
    Am J Hum Genet; 1991 Jan 30; 48(1):53-64. PubMed ID: 1985463
    [Abstract] [Full Text] [Related]

  • 12. Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy.
    Monaco AP, Bertelson CJ, Colletti-Feener C, Kunkel LM.
    Hum Genet; 1987 Mar 30; 75(3):221-7. PubMed ID: 2881877
    [Abstract] [Full Text] [Related]

  • 13. 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 30; 25(2):231-6. PubMed ID: 3777020
    [Abstract] [Full Text] [Related]

  • 14. Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy.
    Boyd Y, Buckle VJ.
    Clin Genet; 1986 Feb 30; 29(2):108-15. PubMed ID: 3955860
    [Abstract] [Full Text] [Related]

  • 15. A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosome.
    van Ommen GJ, Verkerk JM, Hofker MH, Monaco AP, Kunkel LM, Ray P, Worton R, Wieringa B, Bakker E, Pearson PL.
    Cell; 1986 Nov 21; 47(4):499-504. PubMed ID: 2877741
    [Abstract] [Full Text] [Related]

  • 16. 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 21; 50(4):725-41. PubMed ID: 1347968
    [Abstract] [Full Text] [Related]

  • 17. 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 21; 31(4):265-72. PubMed ID: 3594934
    [Abstract] [Full Text] [Related]

  • 18. Physical mapping of a translocation breakpoint in neurofibromatosis.
    Fountain JW, Wallace MR, Bruce MA, Seizinger BR, Menon AG, Gusella JF, Michels VV, Schmidt MA, Dewald GW, Collins FS.
    Science; 1989 Jun 02; 244(4908):1085-7. PubMed ID: 2543076
    [Abstract] [Full Text] [Related]

  • 19. 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; 1989 Jun 02; 318(6047):672-5. PubMed ID: 3001530
    [Abstract] [Full Text] [Related]

  • 20. Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families.
    Dorkins H, Junien C, Mandel JL, Wrogemann K, Moison JP, Martinez M, Old JM, Bundey S, Schwartz M, Carpenter N.
    Hum Genet; 1985 Jun 02; 71(2):103-7. PubMed ID: 2995231
    [Abstract] [Full Text] [Related]

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