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Journal Abstract Search

148 related items for PubMed ID: 2471152

  • 1. 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]

  • 2. 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]

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  • 8. MspI RFLP at 19q12-q13.1 identified by the anonymous DNA sequence p30B18 [D19S31].
    Smeets H, Coerwinkel M, Schepens J, Brunner H, Schonk D, Ropers HH, Wieringa B.
    Nucleic Acids Res; 1989 May 11; 17(9):3627. PubMed ID: 2471158
    [No Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. A rare MspI RFLP of the DMD probe p20 (DXS269).
    Uhlhaas S, Bakker E, van Broeckhoven C, Barth-Schulz A, Friedl W.
    Hum Genet; 1992 Apr 26; 89(1):122. PubMed ID: 1374360
    [No Abstract] [Full Text] [Related]

  • 11. [Use of dystrophin c-DNA for the direct diagnosis of Duchenne muscular dystrophy in female carriers].
    Baiget M, del Río E, Gallano P.
    Neurologia; 1989 Oct 26; 4(8):268-76. PubMed ID: 2576910
    [Abstract] [Full Text] [Related]

  • 12. Dystrophin-related muscular dystrophies.
    Witkowski JA.
    J Child Neurol; 1989 Oct 26; 4(4):251-71. PubMed ID: 2571631
    [Abstract] [Full Text] [Related]

  • 13. Gene mapping and the muscular dystrophies.
    Harper PS.
    Prog Clin Biol Res; 1989 Oct 26; 306():29-49. PubMed ID: 2567999
    [No Abstract] [Full Text] [Related]

  • 14. PvuII RFLPs in the DMD gene detected by a subclone (cDMD1a) of the cDNA.
    Deng HX, Niikawa N.
    Nucleic Acids Res; 1990 May 25; 18(10):3107. PubMed ID: 1971933
    [No Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNA.
    Darras BT, Koenig M, Kunkel LM, Francke U.
    Am J Med Genet; 1988 Mar 25; 29(3):713-26. PubMed ID: 2897793
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  • 17. Brother/sister pairs affected with early-onset, progressive muscular dystrophy: molecular studies reveal etiologic heterogeneity.
    Francke U, Darras BT, Hersh JH, Berg BO, Miller RG.
    Am J Hum Genet; 1989 Jul 25; 45(1):63-72. PubMed ID: 2568091
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  • 18. Duchenne muscular dystrophy: the gene and the protein.
    Love DR, Davies KE.
    Mol Biol Med; 1989 Feb 25; 6(1):7-17. PubMed ID: 2666821
    [No Abstract] [Full Text] [Related]

  • 19. An informative polymorphism detectable by polymerase chain reaction at the 3' end of the dystrophin gene.
    Oudet C, Heilig R, Mandel JL.
    Hum Genet; 1990 Feb 25; 84(3):283-5. PubMed ID: 1968037
    [Abstract] [Full Text] [Related]

  • 20. Normal human genomic restriction-fragment patterns and polymorphisms revealed by hybridization with the entire dystrophin cDNA.
    Darras BT, Francke U.
    Am J Hum Genet; 1988 Nov 25; 43(5):612-9. PubMed ID: 2903662
    [Abstract] [Full Text] [Related]

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