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Journal Abstract Search

147 related items for PubMed ID: 2565028

  • 1. 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
    [No Abstract] [Full Text] [Related]

  • 2. Development of additional RFLP probes near the locus for Duchenne muscular dystrophy by cosmid cloning of the DXS84 (754) locus.
    Hofker MH, van Ommen GJ, Bakker E, Burmeister M, Pearson PL.
    Hum Genet; 1986 Nov 25; 74(3):270-4. PubMed ID: 2877935
    [Abstract] [Full Text] [Related]

  • 3. Duchenne muscular dystrophy (DMD) gene cDNA 8 PstI and TaqI polymorphisms involve exon 51 of the HindIII map.
    Laing NG, Akkari PA, Chandler DC, Thomas HE, Layton MG, Mears ME, Kakulas BA.
    Nucleic Acids Res; 1990 Jul 25; 18(14):4284. PubMed ID: 1974044
    [No Abstract] [Full Text] [Related]

  • 4. 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
    [No Abstract] [Full Text] [Related]

  • 5. 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 26; 22(3):179-81. PubMed ID: 2989525
    [Abstract] [Full Text] [Related]

  • 6. Diagnosis of Duchenne and Becker muscular dystrophies by DNA polymorphism.
    Akita Y, Ohno S, Goto J, Nakano I, Takatsu M, Sugita H, Suzuki K.
    Jinrui Idengaku Zasshi; 1987 Jun 26; 32(2):71-82. PubMed ID: 2893850
    [No Abstract] [Full Text] [Related]

  • 7. 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
    [No Abstract] [Full Text] [Related]

  • 8. Isolation of a random cosmid clone, cX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophy.
    Hofker MH, Bergen AA, Skraastad MI, Bakker E, Francke U, Wieringa B, Bartley J, van Ommen GJ, Pearson PL.
    Hum Genet; 1986 Nov 25; 74(3):275-9. PubMed ID: 2877936
    [Abstract] [Full Text] [Related]

  • 9. Isolation of the gene for Duchenne muscular dystrophy.
    Singh DN.
    Indian J Pediatr; 1988 Nov 25; 55(2):177-82. PubMed ID: 2900215
    [No Abstract] [Full Text] [Related]

  • 10. Carrier detection and gene analysis of Duchenne muscular dystrophy.
    Pearson PL, van Ommen GJ, Bakker E.
    Cold Spring Harb Symp Quant Biol; 1986 Nov 25; 51 Pt 1():353-8. PubMed ID: 2884063
    [No Abstract] [Full Text] [Related]

  • 11. [Uses of RFLP analysis in detecting Duchenne muscular dystrophy gene carrier].
    Chen F.
    Zhonghua Yi Xue Za Zhi; 1991 Jun 25; 71(6):339-41. PubMed ID: 1687519
    [No Abstract] [Full Text] [Related]

  • 12. RFLP for Duchenne muscular dystrophy cDNA clone 44-1.
    Laing NG, Siddique T, Bartlett RJ, Yamaoka LH, Chen JC, Walker AP, Hung WY, Roses AD.
    Nucleic Acids Res; 1988 Jul 25; 16(14B):7209. PubMed ID: 2900496
    [No Abstract] [Full Text] [Related]

  • 13. 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 25; 23(6):531-7. PubMed ID: 2879924
    [Abstract] [Full Text] [Related]

  • 14. Significantly higher frequency of the MspI 2.2 kb allele of the Duchenne muscular dystrophy intragenic probe P-20 in the Chinese population.
    Wei J, Guo Y, Chen B, Yang Y.
    Hum Genet; 1992 Dec 25; 90(1-2):149-50. PubMed ID: 1385293
    [Abstract] [Full Text] [Related]

  • 15. Isolating the gene for Duchenne muscular dystrophy.
    Harper PS.
    Br Med J (Clin Res Ed); 1986 Sep 27; 293(6550):773-4. PubMed ID: 2876742
    [No Abstract] [Full Text] [Related]

  • 16. [Detection of dystrophin gene mutation carrier state].
    Bisko M, Zimowski JG, Fidziańska E, Badurska B, Fidziańska A, Hausmanowa-Petrusewicz I, Zaremba J.
    Neurol Neurochir Pol; 1996 Sep 27; 30(2):193-9; quiz 200. PubMed ID: 8756246
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Molecular analysis of human muscular dystrophies.
    Davies KE, Forrest S, Smith T, Kenwrick S, Ball S, Dorkins H, Patterson M.
    Muscle Nerve; 1987 Sep 27; 10(3):191-9. PubMed ID: 2882417
    [Abstract] [Full Text] [Related]

  • 19. X-chromosome-specific polymorphisms in Duchenne muscular dystrophy: clinical applications.
    O'Brien T.
    Biochem Soc Trans; 1984 Jun 27; 12(3):371-2. PubMed ID: 6734896
    [No Abstract] [Full Text] [Related]

  • 20. X-linked muscular dystrophies: studies through functional assay and DNA polymorphisms.
    Romeo G, Rocchi M, Roncuzzi L, Ferlini A, Nobile C, Rugolo M.
    Adv Neurol; 1988 Jun 27; 48():31-6. PubMed ID: 2891257
    [No Abstract] [Full Text] [Related]

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