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Journal Abstract Search

130 related items for PubMed ID: 2893850

  • 1. 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; 32(2):71-82. PubMed ID: 2893850
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  • 3. [Carrier detection and gene analysis in a Duchenne muscular dystrophy family].
    Lu FM.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1990 Aug; 23(4):231-3, 255. PubMed ID: 1979269
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  • 4. Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.
    Sugino S, Fujishita S, Kamimura N, Matsumoto T, Wapenaar MC, Deng HX, Shibuya N, Miike T, Niikawa N.
    Am J Med Genet; 1989 Dec; 34(4):555-61. PubMed ID: 2576185
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  • 5. [Uses of RFLP analysis in detecting Duchenne muscular dystrophy gene carrier].
    Chen F.
    Zhonghua Yi Xue Za Zhi; 1991 Jun; 71(6):339-41. PubMed ID: 1687519
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  • 7. [DNA diagnosis of muscular dystrophies].
    Lindlöf M, Somer H.
    Duodecim; 1988 Jun; 104(22):1787-95. PubMed ID: 2905983
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  • 10. Molecular analysis of human muscular dystrophies.
    Davies KE, Forrest S, Smith T, Kenwrick S, Ball S, Dorkins H, Patterson M.
    Muscle Nerve; 1987 Jun; 10(3):191-9. PubMed ID: 2882417
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  • 17. Towards a complete linkage map of the human X chromosome.
    Davies KE, Williamson R.
    Horiz Biochem Biophys; 1986 Jun; 8():1-50. PubMed ID: 2875929
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  • 19. [Molecular genetic research on Duchenne-Becker myodystrophy. The correlation of the severity of the disease with the type of deletion].
    Badalian LO, Malygina NA.
    Zh Nevrol Psikhiatr Im S S Korsakova; 1995 Jun; 95(6):90-2. PubMed ID: 8788991
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  • 20. DNA diagnostic tests in Xp21 dystrophy families for prenatal diagnosis.
    Dinçer P, Topaloğlu H, Ayter S.
    Turk J Pediatr; 1998 Jun; 40(3):347-55. PubMed ID: 9763898
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