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Journal Abstract Search

146 related items for PubMed ID: 2914705

  • 1. 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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  • 2. A cDNA clone from the Duchenne/Becker muscular dystrophy gene.
    Burghes AH, Logan C, Hu X, Belfall B, Worton RG, Ray PN.
    Nature; 1989 Jan; 328(6129):434-7. PubMed ID: 3614347
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  • 10. 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; 33(4):513-8. PubMed ID: 7258185
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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; 18(6):442-7. PubMed ID: 7334502
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  • 14. Mapping of X chromosome translocation breakpoints in females with Duchenne muscular dystrophy with respect to exons of the dystrophin gene.
    Cockburn DJ, Munro EA, Craig IW, Boyd Y.
    Hum Genet; 1992 Dec; 90(4):407-12. PubMed ID: 1483697
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  • 15. 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; 1(4):329-36. PubMed ID: 2896627
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  • 16. Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations.
    Darras BT, Blattner P, Harper JF, Spiro AJ, Alter S, Francke U.
    Am J Hum Genet; 1988 Nov; 43(5):620-9. PubMed ID: 2903663
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  • 17. 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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  • 18. 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; 20(6):461-3. PubMed ID: 6655672
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  • 20. 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; 1983 Dec; 318(6047):672-5. PubMed ID: 3001530
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