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Journal Abstract Search

96 related items for PubMed ID: 1687519

  • 21. A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected male.
    Darras BT, Francke U.
    Nature; ; 329(6139):556-8. PubMed ID: 2889145
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  • 22. Molecular deletion analysis in Duchenne muscular dystrophy.
    Thomas NS, Ray PN, Worton RG, Harper PS.
    J Med Genet; 1986 Dec; 23(6):509-15. PubMed ID: 2879923
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  • 23. RFLP for HindIII at the Duchenne muscular dystrophy gene.
    Prior TW, Friedman KJ, Silverman LM.
    Nucleic Acids Res; 1989 Mar 25; 17(6):2370. PubMed ID: 2565028
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  • 25. RFLP for Duchenne muscular dystrophy cDNA clone 30-2.
    Walker AP, Bartlett RJ, Laing NG, Siddique T, Yamaoka LH, Chen JC, Hung WY, Roses AD.
    Nucleic Acids Res; 1988 Sep 26; 16(18):9072. PubMed ID: 2902573
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  • 32. Isolation of the gene for Duchenne muscular dystrophy.
    Singh DN.
    Indian J Pediatr; 1988 Sep 26; 55(2):177-82. PubMed ID: 2900215
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  • 34. MspI RFLP for Duchenne muscular dystrophy cDNA subclone 9.
    Wagner M, Reiss J, Hentemann M, Thies U.
    Nucleic Acids Res; 1989 Apr 25; 17(8):3328. PubMed ID: 2471152
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  • 35. Familial inheritance of a DXS164 deletion mutation from a heterozygous female.
    Lanman JT, Pericak-Vance MA, Bartlett RJ, Chen JC, Yamaoka L, Koh J, Speer MC, Hung WY, Roses AD.
    Am J Hum Genet; 1987 Aug 25; 41(2):138-44. PubMed ID: 2887110
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  • 36. [Use of DNA analysis in the prevention of progressive muscular dystrophies].
    Kádasi L, Ferák V, Thurzová M, Kvasnicová M.
    Bratisl Lek Listy; 1988 Nov 25; 89(11):828-34. PubMed ID: 2904832
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  • 37. DNA probes for carrier identification in Duchenne muscular dystrophy.
    Worton RG.
    Clin Chem; 1989 Apr 25; 35(4):519-20. PubMed ID: 2564816
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  • 40. Duchenne muscular dystrophy--a molecular service.
    Ballo R, Hitzeroth HW, Beighton PH.
    S Afr Med J; 1991 Feb 16; 79(4):209-12. PubMed ID: 1671720
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