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Journal Abstract Search

295 related items for PubMed ID: 1684391

  • 1. 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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  • 3. 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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  • 4. 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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  • 5. 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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  • 6. Intragenic DNA polymorphism analysis of DMD/BMD dystrophy gene for carrier and prenatal diagnosis in 60 Iranian healthy individuals.
    Zamani M, Salahshour V, Kollaee A, Zamani GR, Sheidai M, Mohammadi M, Ghaffarpor M.
    Int J Neurosci; 2011 Oct; 121(10):551-6. PubMed ID: 21774744
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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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  • 8. Southern blot and PCR analyses of dystrophin gene deletions in Japanese patients with Duchenne muscular dystrophy.
    Nakajima T, Matsuo M, Nakamura H, Fujiwara Y.
    Kobe J Med Sci; 1991 Feb; 37(1):21-33. PubMed ID: 1921260
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  • 9. [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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  • 12. 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; 51(2):223-6. PubMed ID: 14571009
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  • 13. DNA polymorphisms and deletion analysis of the Duchenne-Becker muscular dystrophy gene in the Chinese.
    Soong BW, Tsai TF, Su CH, Kao KP, Hsiao KJ, Su TS.
    Am J Med Genet; 1991 Mar 15; 38(4):593-600. PubMed ID: 1676564
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  • 14. Identification of female carriers for Duchenne and Becker muscular dystrophies using a FISH-based approach.
    Ligon AH, Kashork CD, Richards CS, Shaffer LG.
    Eur J Hum Genet; 2000 Apr 15; 8(4):293-8. PubMed ID: 10854113
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  • 16. Molecular deletion patterns in Duchenne muscular dystrophy patients.
    Lucotte G, David F, Levy C.
    Ann Genet; 1989 Apr 15; 32(4):214-9. PubMed ID: 2610487
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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 15; 19(2):108-12. PubMed ID: 19084397
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  • 19. 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 15; 36(4):317-24. PubMed ID: 1811098
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  • 20. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients.
    Shomrat R, Gluck E, Legum C, Shiloh Y.
    Am J Med Genet; 1994 Feb 15; 49(4):369-73. PubMed ID: 8160727
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