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Journal Abstract Search

88 related items for PubMed ID: 2193159

  • 1. Dystrophin expression and genotypic analysis of two cases of benign X linked myopathy (McLeod's syndrome).
    Carter ND, Morgan JE, Monaco AP, Schwartz MS, Jeffery S.
    J Med Genet; 1990 Jun; 27(6):345-7. PubMed ID: 2193159
    [Abstract] [Full Text] [Related]

  • 2. Normal dystrophin in McLeod myopathy.
    Danek A, Witt TN, Stockmann HB, Weiss BJ, Schotland DL, Fischbeck KH.
    Ann Neurol; 1990 Nov; 28(5):720-2. PubMed ID: 2260862
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  • 3. Localization of the McLeod locus (XK) within Xp21 by deletion analysis.
    Bertelson CJ, Pogo AO, Chaudhuri A, Marsh WL, Redman CM, Banerjee D, Symmans WA, Simon T, Frey D, Kunkel LM.
    Am J Hum Genet; 1988 May; 42(5):703-11. PubMed ID: 3358422
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  • 4. Myopathy in complex glycerol kinase deficiency patients is due to 3' deletions of the dystrophin gene.
    Darras BT, Francke U.
    Am J Hum Genet; 1988 Aug; 43(2):126-30. PubMed ID: 2840818
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  • 5. Familial X-linked myalgia and cramps: a nonprogressive myopathy associated with a deletion in the dystrophin gene.
    Gospe SM, Lazaro RP, Lava NS, Grootscholten PM, Scott MO, Fischbeck KH.
    Neurology; 1989 Oct; 39(10):1277-80. PubMed ID: 2677830
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  • 6. Skewed X inactivation in a female MZ twin results in Duchenne muscular dystrophy.
    Richards CS, Watkins SC, Hoffman EP, Schneider NR, Milsark IW, Katz KS, Cook JD, Kunkel LM, Cortada JM.
    Am J Hum Genet; 1990 Apr; 46(4):672-81. PubMed ID: 2180286
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  • 9. [Use of dystrophin c-DNA for the direct diagnosis of Duchenne muscular dystrophy in female carriers].
    Baiget M, del Río E, Gallano P.
    Neurologia; 1989 Oct; 4(8):268-76. PubMed ID: 2576910
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  • 10. 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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  • 12. Fine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21.
    Ho MF, Monaco AP, Blonden LA, van Ommen GJ, Affara NA, Ferguson-Smith MA, Lehrach H.
    Am J Hum Genet; 1992 Feb; 50(2):317-30. PubMed ID: 1734714
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  • 14. The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs.
    Cooper BJ, Winand NJ, Stedman H, Valentine BA, Hoffman EP, Kunkel LM, Scott MO, Fischbeck KH, Kornegay JN, Avery RJ.
    Nature; 1988 Jul 14; 334(6178):154-6. PubMed ID: 3290691
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  • 15. Complementary DNA probes for the Duchenne muscular dystrophy locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasia.
    McCabe ER, Towbin J, Chamberlain J, Baumbach L, Witkowski J, van Ommen GJ, Koenig M, Kunkel LM, Seltzer WK.
    J Clin Invest; 1989 Jan 14; 83(1):95-9. PubMed ID: 2536049
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  • 16. 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 14; 27(3):145-50. PubMed ID: 2182872
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  • 18. Clinical and molecular studies in Duchenne muscular dystrophy.
    Emery AE.
    Prog Clin Biol Res; 1989 Mar 14; 306():15-28. PubMed ID: 2662210
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  • 20. Feline muscular dystrophy with dystrophin deficiency.
    Carpenter JL, Hoffman EP, Romanul FC, Kunkel LM, Rosales RK, Ma NS, Dasbach JJ, Rae JF, Moore FM, McAfee MB.
    Am J Pathol; 1989 Nov 14; 135(5):909-19. PubMed ID: 2683799
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