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Journal Abstract Search

126 related items for PubMed ID: 3275902

  • 1. Duchenne muscular dystrophy: high frequency of deletions.
    Bartlett RJ, Pericak-Vance MA, Koh J, Yamaoka LH, Chen JC, Hung WY, Speer MC, Wapenaar MC, Van Ommen GJ, Bakker E.
    Neurology; 1988 Jan; 38(1):1-4. PubMed ID: 3275902
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  • 2. Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNA.
    Upadhyaya M, Smith RA, Thomas NS, Norman AM, Harper PS.
    Clin Genet; 1990 Jun; 37(6):456-62. PubMed ID: 2200624
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  • 3. Deletion screening in patients with Duchenne muscular dystrophy.
    Wulff K, Herrmann FH, Wapenaar MC, Wehnert M.
    J Neurol; 1989 Dec; 236(8):470-3. PubMed ID: 2614492
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  • 6. Deletion analysis of Duchenne muscular dystrophy using cDNA probes and multiplex PCR.
    Radosavljević D, Todorović D, Crkvenjakov R.
    Neurol Croat; 1991 Dec; 40(3):157-64. PubMed ID: 1681950
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  • 8. Deletion screening and prenatal diagnosis of Duchenne muscular dystrophy using cDNA probes Cf 23a and Cf 56a.
    Herrmann FH, Wulff K, Schütz M, Wehnert M.
    Eur J Pediatr; 1990 Jan; 149(4):263-5. PubMed ID: 1968008
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  • 9. 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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  • 10. 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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  • 11. Carrier diagnosis of Duchenne muscular dystrophy using restriction fragment length polymorphisms.
    Hejtmancik JF, Harris SG, Tsao CC, Ward PA, Caskey CT.
    Neurology; 1986 Dec 07; 36(12):1553-62. PubMed ID: 2878392
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  • 17. DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.
    Bakker E, Bonten EJ, De Lange LF, Veenema H, Majoor-Krakauer D, Hofker MH, Van Ommen GJ, Pearson PL.
    J Med Genet; 1986 Dec 07; 23(6):573-80. PubMed ID: 2879929
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