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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

278 related items for PubMed ID: 7334502

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  • 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(6):516-22. PubMed ID: 3742857
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  • 11. Mapping of four translocation breakpoints within the Duchenne muscular dystrophy gene.
    Bodrug SE, Burghes AH, Ray PM, Worton RG.
    Genomics; 1989 Jan; 4(1):101-4. PubMed ID: 2914705
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  • 13. 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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  • 14. Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm.
    Lindenbaum RH, Clarke G, Patel C, Moncrieff M, Hughes JT.
    J Med Genet; 1979 Oct 25; 16(5):389-92. PubMed ID: 513085
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  • 15. Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome.
    Verellen-Dumoulin C, Freund M, De Meyer R, Laterre C, Frédéric J, Thompson MW, Markovic VD, Worton RG.
    Hum Genet; 1984 Oct 25; 67(1):115-9. PubMed ID: 6745920
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  • 16. High-resolution banding study of an X/4 translocation in a female with Duchenne muscular dystrophy.
    Saito F, Tonomura A, Kimura S, Misugi N, Sugita H.
    Hum Genet; 1985 Oct 25; 71(4):370-1. PubMed ID: 4077054
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  • 17. 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; 1985 Oct 25; 318(6047):672-5. PubMed ID: 3001530
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  • 19. 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 25; 3(4):315-22. PubMed ID: 3243546
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  • 20. 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
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