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PUBMED FOR HANDHELDS

Journal Abstract Search


146 related items for PubMed ID: 2900215

  • 1. Isolation of the gene for Duchenne muscular dystrophy.
    Singh DN.
    Indian J Pediatr; 1988; 55(2):177-82. PubMed ID: 2900215
    [No Abstract] [Full Text] [Related]

  • 2. Linkage analysis of a DNA polymorphism proximal to the Duchenne and Becker muscular dystrophy loci on the short arm of the X chromosome.
    Brown CS, Pearson PL, Thomas NS, Sarfarazi M, Harper PS, Shaw DJ.
    J Med Genet; 1985 Jun; 22(3):179-81. PubMed ID: 2989525
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  • 3. Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families.
    Bertelson CJ, Bartley JA, Monaco AP, Colletti-Feener C, Fischbeck K, Kunkel LM.
    J Med Genet; 1986 Dec; 23(6):531-7. PubMed ID: 2879924
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  • 4. The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy.
    Harper PS, O'Brien T, Murray JM, Davies KE, Pearson P, Williamson R.
    J Med Genet; 1983 Aug; 20(4):252-4. PubMed ID: 6684693
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  • 6. Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome.
    Kingston HM, Thomas NS, Pearson PL, Sarfarazi M, Harper PS.
    J Med Genet; 1983 Aug; 20(4):255-8. PubMed ID: 6620324
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  • 8. 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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  • 10. Carrier detection and gene analysis of Duchenne muscular dystrophy.
    Pearson PL, van Ommen GJ, Bakker E.
    Cold Spring Harb Symp Quant Biol; 1986 Mar 25; 51 Pt 1():353-8. PubMed ID: 2884063
    [No Abstract] [Full Text] [Related]

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  • 12. 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
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  • 14. 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 Nov 21; 70(2):148-56. PubMed ID: 2989153
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  • 15. Gene mapping and the muscular dystrophies.
    Harper PS.
    Prog Clin Biol Res; 1989 Nov 21; 306():29-49. PubMed ID: 2567999
    [No Abstract] [Full Text] [Related]

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  • 18. Linkage studies in Duchenne and Becker muscular dystrophies.
    Walker A, Hart K, Cole C, Hodgson S, Johnson L, Dubowitz V, Bobrow M.
    J Med Genet; 1986 Dec 21; 23(6):538-47. PubMed ID: 2879925
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  • 20. Genetic linkage relationship between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophy.
    Sarfarazi M, Harper PS, Kingston HM, Murray JM, O'Brien T, Davies KE, Williamson R, Tippett P, Sanger R.
    Hum Genet; 1983 Dec 21; 65(2):169-71. PubMed ID: 6317539
    [Abstract] [Full Text] [Related]


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