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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

295 related items for PubMed ID: 1684391

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  • 23. [Carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy by PCR methods].
    Tsukamoto H, Inui K, Okada S.
    Nihon Rinsho; 1993 Sep; 51(9):2428-34. PubMed ID: 8105117
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  • 24. Possibilities and limitations of carrier diagnosis in families with Duchenne muscular dystrophy caused by deletions in the major hot spot region using pulsed-field gel electrophoresis.
    Huschenbett J, Volz A, Pfeifer L, Speer A.
    Biomed Biochim Acta; 1991 Sep; 50(12):1205-12. PubMed ID: 1824538
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  • 25. Application of DNA probes to carrier detection and prenatal diagnosis of Duchenne (and Becker) muscular dystrophy.
    Mulley JC, Gedeon AK, Haan EA, Sheffield LJ, White SJ, Bates LJ, Robertson EF, Sutherland GR.
    Aust Paediatr J; 1988 Sep; 24 Suppl 1():92-7. PubMed ID: 3202740
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  • 27. Experience with DNA analysis in Duchenne and Becker muscular dystrophy families in NSW.
    Morgan G, Donald JA, Chen J, Serravalle S, Colley P, Denton MJ.
    Aust Paediatr J; 1988 Sep; 24 Suppl 1():98-9. PubMed ID: 3202741
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  • 28. Preferential deletion of exons in Duchenne and Becker muscular dystrophies.
    Forrest SM, Cross GS, Speer A, Gardner-Medwin D, Burn J, Davies KE.
    Nature; 1988 Sep; 329(6140):638-40. PubMed ID: 2821406
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  • 30. Screening of deletions and RFLP analysis in Turkish DMD/BMD families by PCR.
    Gökgöz N, Kuseyri F, Topaloğlu H, Yüksel-Apak M, Kirdar B.
    Clin Genet; 1993 May; 43(5):261-6. PubMed ID: 8104108
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  • 31. Molecular deletion patterns in Duchenne and Becker type muscular dystrophy.
    Liechti-Gallati S, Koenig M, Kunkel LM, Frey D, Boltshauser E, Schneider V, Braga S, Moser H.
    Hum Genet; 1989 Mar; 81(4):343-8. PubMed ID: 2784778
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  • 33. Allele frequencies of intragenic, and 5' and 3' markers of the dystrophin gene in Japanese families afflicted with Duchenne or Becker muscular dystrophy.
    Tsukamoto H, Inui K, Fukushima H, Okada S.
    Jpn J Hum Genet; 1996 Dec; 41(4):391-7. PubMed ID: 9088109
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  • 39. Carrier detection of Duchenne/Becker muscular dystrophy by using fluorescent linkage analysis in Taiwan.
    Lee CC, Wu MC, Wu JY, Li TC, Tsai FJ, Tsai CH.
    Acta Paediatr Taiwan; 2000 Dec; 41(2):69-74. PubMed ID: 10927942
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