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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

232 related items for PubMed ID: 1353862

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  • 4. Somatic mosaicism at the Duchenne locus.
    Lebo RV, Olney RK, Golbus MS.
    Am J Med Genet; 1990 Oct; 37(2):187-90. PubMed ID: 1978985
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  • 6. Identification of carriers of Duchenne muscular dystrophy: value of molecular analysis.
    LeRoy BS, Uhrhammer NA, Steere KJ, Boehm CD, King RA, Rich SS, Williams PP, Smith SA, de Martinville B.
    Am J Med Genet; 1988 Nov; 31(3):709-21. PubMed ID: 2906525
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  • 7. 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; 29(3):713-26. PubMed ID: 2897793
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  • 17. Heteroduplex analysis of the dystrophin gene: application to point mutation and carrier detection.
    Prior TW, Papp AC, Snyder PJ, Sedra MS, Western LM, Bartolo C, Moxley RT, Mendell JR.
    Am J Med Genet; 1994 Mar 01; 50(1):68-73. PubMed ID: 8160755
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  • 18. Myocardial evidence of dystrophin mosaic in a Duchenne muscular dystrophy carrier.
    Schmidt-Achert M, Fischer P, Pongratz D.
    Lancet; 1992 Nov 14; 340(8829):1235-6. PubMed ID: 1359314
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