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Journal Abstract Search

286 related items for PubMed ID: 1979269

  • 1. [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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  • 5. Possibilities and problems in genomic diagnosis of Duchenne muscular dystrophy with molecular probes.
    Speer A, Davies K, McGlade S, Hanke R, Spiegler AW, Szibor R, Sommer D, Herrmann F, Coutelle C.
    Biomed Biochim Acta; 1986 Aug; 45(7):K19-27. PubMed ID: 2878658
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  • 6. [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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  • 8. A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome.
    Wood S, Shukin RJ, McGillivray BC, Ray PN, Worton RG.
    Am J Med Genet; 1988 Feb; 29(2):419-23. PubMed ID: 2895584
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  • 13. 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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  • 14. Carrier detection by DNA analysis in Duchenne muscular dystrophy families.
    Battaloğlu E, Telatar M, Deymeer F, Serdaroğlu P, Ozdemir C, Kuseyri F, Apak MY, Tolun A.
    Turk J Pediatr; 1992 Mar; 34(2):79-92. PubMed ID: 1440954
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  • 16. Evaluation of carrier detection rates for Duchenne and Becker muscular dystrophies using serum creatine-kinase (CK) and pyruvate-kinase (PK) through discriminant analysis.
    Zatz M, Otto PA.
    Am J Med Genet; 1986 Oct; 25(2):219-30. PubMed ID: 3777019
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  • 17. 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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  • 18. 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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