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Journal Abstract Search

266 related items for PubMed ID: 1536162

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  • 2. 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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  • 4. DNA analysis of Duchenne and Becker muscular dystrophy using pERT87 genomic probes and dystrophin cDNA probes--establishing the optimum strategy for carrier diagnosis in the Japanese population.
    Ubagai T, Katayama S.
    Jinrui Idengaku Zasshi; 1991 Sep; 36(3):211-27. PubMed ID: 1684391
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  • 6. [Genotypic diagnosis of Duchenne and Becker muscular dystrophies].
    Tuffery-Giraud S, Chambert S, Demaille J, Claustres M.
    Ann Biol Clin (Paris); 1999 Sep; 57(4):417-26. PubMed ID: 10432364
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  • 7. Case of the month: germline mosaicism in carriers of Duchenne muscular dystrophy.
    Prior TW, Papp AC, Snyder PJ, Mendell JR.
    Muscle Nerve; 1992 Aug; 15(8):960-3. PubMed ID: 1353862
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  • 9. Somatic mosaicism at the Duchenne locus.
    Lebo RV, Olney RK, Golbus MS.
    Am J Med Genet; 1990 Oct; 37(2):187-90. PubMed ID: 1978985
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  • 11. 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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  • 12. Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction.
    Fujishita S, Shibuya N, Niikawa N, Nagataki S.
    Jinrui Idengaku Zasshi; 1991 Dec; 36(4):317-24. PubMed ID: 1811098
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  • 13. Heteroduplex analysis of the dystrophin gene: application to point mutation and carrier detection.
    Prior TW, Papp AC, Snyder PJ, Sedra MS, Western LM, Bartolo C, Moxley RT, Mendell JR.
    Am J Med Genet; 1994 Mar 01; 50(1):68-73. PubMed ID: 8160755
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  • 14. Deletion analysis of the dystrophin gene in Duchenne and Becker muscular dystrophy patients: use in carrier diagnosis.
    Kumari D, Mital A, Gupta M, Goyle S.
    Neurol India; 2003 Jun 01; 51(2):223-6. PubMed ID: 14571009
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  • 17. Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families - detection of carrier status in symptomatic and asymptomatic female relatives.
    Pikó H, Vancsó V, Nagy B, Bán Z, Herczegfalvi A, Karcagi V.
    Neuromuscul Disord; 2009 Feb 01; 19(2):108-12. PubMed ID: 19084397
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  • 18. Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boy.
    Tuffery S, Moine P, Sarda P, Lefort G, Boulot P, Demaille J, Claustres M.
    Genet Couns; 1994 Feb 01; 5(2):183-5. PubMed ID: 7917130
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  • 20. Identification of a point mutation and germinal mosaicism in a Duchenne muscular dystrophy family.
    Wilton SD, Chandler DC, Kakulas BA, Laing NG.
    Hum Mutat; 1994 Feb 01; 3(2):133-40. PubMed ID: 8199594
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