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Journal Abstract Search

127 related items for PubMed ID: 2182872

  • 1. Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115.
    Passos-Bueno MR, Rapaport D, Love D, Flint T, Bortolini ER, Zatz M, Davies KE.
    J Med Genet; 1990 Mar; 27(3):145-50. PubMed ID: 2182872
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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. Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophy.
    Rapaport D, Passos-Bueno MR, Brandão L, Love D, Vainzof M, Zatz M.
    Am J Med Genet; 1991 Jun 15; 39(4):437-41. PubMed ID: 1877622
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  • 7. Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes.
    Cooke A, Lanyon WG, Wilcox DE, Dornan ES, Kataki A, Gillard EF, McWhinnie AJ, Morris A, Ferguson-Smith MA, Connor JM.
    J Med Genet; 1990 May 15; 27(5):292-7. PubMed ID: 2191136
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  • 9. Distinction of Becker from limb-girdle muscular dystrophy by means of dystrophin cDNA probes.
    Norman A, Thomas N, Coakley J, Harper P.
    Lancet; 1989 Mar 04; 1(8636):466-8. PubMed ID: 2563842
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  • 11. Patterns of exon deletions in Duchenne and Becker muscular dystrophy.
    Read AP, Mountford RC, Forrest SM, Kenwrick SJ, Davies KE, Harris R.
    Hum Genet; 1988 Oct 04; 80(2):152-6. PubMed ID: 3169738
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  • 14. 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 04; 29(3):713-26. PubMed ID: 2897793
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