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Journal Abstract Search

276 related items for PubMed ID: 2879923

  • 1. Molecular deletion analysis in Duchenne muscular dystrophy.
    Thomas NS, Ray PN, Worton RG, Harper PS.
    J Med Genet; 1986 Dec; 23(6):509-15. PubMed ID: 2879923
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  • 2. Prenatal diagnosis and carrier detection by DNA studies in a Duchenne muscular dystrophy family with no living affected male.
    Chen JD, Denton MJ, Serravalle S, Morgan G.
    Aust Paediatr J; 1988 Dec; 24(6):351-3. PubMed ID: 2907402
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  • 3. Deletion analysis for Duchenne (and Becker) muscular dystrophy.
    Kimber RD, Hyland VJ, Haan EA, Mulley JC.
    Aust Paediatr J; 1989 Oct; 25(5):292-5. PubMed ID: 2590130
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  • 4. Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy.
    Thompson MW, Ray PN, Belfall B, Duff C, Logan C, Oss I, Worton RG.
    J Med Genet; 1986 Dec; 23(6):548-55. PubMed ID: 2879926
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  • 8. Analysis of RFLPs and DNA deletions in the Chinese Duchenne muscular dystrophy gene.
    Zeng YT, Chen MJ, Ren ZR, Qui XK, Huang SZ.
    J Med Genet; 1991 Mar; 28(3):167-70. PubMed ID: 1675685
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  • 9. Molecular analysis of 25 Chinese families with Duchenne/Becker muscular dystrophy.
    Ko TM, Chen CF, Chiu HC, Hsieh FJ, Lee TY.
    J Formos Med Assoc; 1990 Oct; 89(10):850-6. PubMed ID: 1981771
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  • 10. Linkage studies in Duchenne and Becker muscular dystrophies.
    Walker A, Hart K, Cole C, Hodgson S, Johnson L, Dubowitz V, Bobrow M.
    J Med Genet; 1986 Dec; 23(6):538-47. PubMed ID: 2879925
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  • 12. Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.
    Davies KE, Smith TJ, Bundey S, Read AP, Flint T, Bell M, Speer A.
    J Med Genet; 1988 Jan; 25(1):9-13. PubMed ID: 3162536
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  • 13. The diagnosis of Duchenne and Becker muscular dystrophies: two years' experience in a comprehensive carrier screening and prenatal diagnostic laboratory.
    Laing NG, Mears ME, Chandler DC, Layton MG, Thomas HE, Johnsen RD, Goldblatt J, Kakulas BA.
    Med J Aust; 1991 Jan 07; 154(1):14-8. PubMed ID: 1670611
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  • 17. 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 07; 81(4):343-8. PubMed ID: 2784778
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  • 18. Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy.
    Monaco AP, Bertelson CJ, Colletti-Feener C, Kunkel LM.
    Hum Genet; 1987 Mar 07; 75(3):221-7. PubMed ID: 2881877
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  • 19. [Carrier detection and gene analysis in a Duchenne muscular dystrophy family].
    Lu FM.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1990 Aug 07; 23(4):231-3, 255. PubMed ID: 1979269
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