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Journal Abstract Search

155 related items for PubMed ID: 1415325

  • 1. Five years experience of predictive testing for myotonic dystrophy using linked DNA markers.
    Reardon W, Floyd JL, Myring J, Lazarou LP, Meredith AL, Harper PS.
    Am J Med Genet; 1992 Aug 01; 43(6):1006-11. PubMed ID: 1415325
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  • 4. Preclinical detection in Japanese families with myotonic dystrophy using polymorphic DNA markers.
    Takemoto Y, Miki T, Nakura J, Nishikawa K, Kamino K, Takeda S, Kuzu K, Osame M, Nakagawa M, Higuchi I.
    Jinrui Idengaku Zasshi; 1989 Sep 01; 34(3):189-94. PubMed ID: 2576756
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  • 9. [Neonatal Steinert's disease: apropos of 2 cases in 2 successive generations].
    Bétrémieux P, Blin-Jezequel E, Lefrançois C, Le Marec B.
    J Genet Hum; 1985 Jan 01; 33(1):21-30. PubMed ID: 3856628
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  • 11. Genetic counselling for myotonic dystrophy: a comparison of lens examination and DNA linkage studies.
    Longstaff S, Curtis D, Quick J, Talbot J.
    Eye (Lond); 1991 Jan 01; 5 ( Pt 1)():93-8. PubMed ID: 1676377
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  • 19. Usefulness of chromosome 19 RFLP haplotypes in the diagnosis of myotonic dystrophy.
    Nokelainen PT, Alanen-Kurki L, Somer HV, Pihko SH, Peltonen L.
    Muscle Nerve; 1991 May 01; 14(5):451-6. PubMed ID: 1678492
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