These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

241 related items for PubMed ID: 3001530

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. 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; 48(1):28-34. PubMed ID: 3180845
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. 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]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. 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 29; 29(6):516-22. PubMed ID: 3742857
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. 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 30; 27(7):426-32. PubMed ID: 2395160
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome.
    Davies KE, Pearson PL, Harper PS, Murray JM, O'Brien T, Sarfarazi M, Williamson R.
    Nucleic Acids Res; 1983 Apr 25; 11(8):2303-12. PubMed ID: 6304647
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy.
    Hofker MH, Wapenaar MC, Goor N, Bakker E, van Ommen GJ, Pearson PL.
    Hum Genet; 1985 Apr 25; 70(2):148-56. PubMed ID: 2989153
    [Abstract] [Full Text] [Related]

  • 17. Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndrome.
    Ellison KA, Roth EJ, McCabe ER, Chinault AC, Zoghbi HY.
    Am J Med Genet; 1993 Nov 15; 47(7):1124-34. PubMed ID: 8291533
    [Abstract] [Full Text] [Related]

  • 18. Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy.
    Thompson MW, Ray PN, Belfall B, Duff C, Logan C, Oss I, Worton RG.
    J Med Genet; 1986 Dec 15; 23(6):548-55. PubMed ID: 2879926
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Long-range restriction map around the Duchenne muscular dystrophy gene.
    Burmeister M, Lehrach H.
    Nature; 1986 Dec 15; 324(6097):582-5. PubMed ID: 3024018
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.