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Journal Abstract Search

180 related items for PubMed ID: 8329890

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  • 3. Prediction of dystrophin phenotype by DNA analysis in Duchenne/Becker muscular dystrophy.
    Specht LA, Beggs AH, Korf B, Kunkel LM, Shapiro F.
    Pediatr Neurol; 1992; 8(6):432-6. PubMed ID: 1476571
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  • 4. Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?
    Vainzof M, Takata RI, Passos-Bueno MR, Pavanello RC, Zatz M.
    Hum Mol Genet; 1993 Jan; 2(1):39-42. PubMed ID: 8490621
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  • 6. Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of Duchenne's and Becker muscular dystrophies of different ages.
    Vainzof M, Pavanello RC, Pavanello I, Tsanaclis AM, Levy JA, Passos-Bueno MR, Rapaport D, Zatz M.
    Neuromuscul Disord; 1991 Jan; 1(3):177-83. PubMed ID: 1822792
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  • 7. Muscle X-inactivation patterns and dystrophin expression in Duchenne muscular dystrophy carriers.
    Matthews PM, Benjamin D, Van Bakel I, Squier MV, Nicholson LV, Sewry C, Barnes PR, Hopkin J, Brown R, Hilton-Jones D.
    Neuromuscul Disord; 1995 May; 5(3):209-20. PubMed ID: 7633186
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  • 8. Manifesting carrier of Becker muscular dystrophy (BMD): clinical and recombinant DNA studies.
    Ionasescu VV, Searby CC, Ionasescu R.
    Acta Neurol Scand; 1989 Jun; 79(6):500-3. PubMed ID: 2782030
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  • 9. Manifesting carriers of Xp21 muscular dystrophy; lack of correlation between dystrophin expression and clinical weakness.
    Sewry CA, Sansome A, Clerk A, Sherratt TG, Hasson N, Rodillo E, Heckmatt JZ, Strong PN, Dubowitz V.
    Neuromuscul Disord; 1993 Mar; 3(2):141-8. PubMed ID: 8358239
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  • 10. Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers.
    Sumita DR, Vainzof M, Campiotto S, Cerqueira AM, Cánovas M, Otto PA, Passos-Bueno MR, Zatz M.
    Am J Med Genet; 1998 Dec 04; 80(4):356-61. PubMed ID: 9856563
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  • 11. Carrier detection of Duchenne and Becker muscular dystrophy using muscle dystrophin immunohistochemistry.
    Oliveira AS, Gabbai AA, Schmidt B, Kiyomoto BH, Lima JG, Minetti C, Bonilla E.
    Arq Neuropsiquiatr; 1992 Dec 04; 50(4):478-85. PubMed ID: 1309152
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  • 12. Discordance of muscular dystrophy in monozygotic female twins: evidence supporting asymmetric splitting of the inner cell mass in a manifesting carrier of Duchenne dystrophy.
    Lupski JR, Garcia CA, Zoghbi HY, Hoffman EP, Fenwick RG.
    Am J Med Genet; 1991 Sep 01; 40(3):354-64. PubMed ID: 1683155
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  • 13. Genetic abnormalities in Duchenne and Becker dystrophies: clinical correlations.
    Medori R, Brooke MH, Waterston RH.
    Neurology; 1989 Apr 01; 39(4):461-5. PubMed ID: 2648185
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  • 14. Uniparental disomy of the entire X chromosome in a female with Duchenne muscular dystrophy.
    Quan F, Janas J, Toth-Fejel S, Johnson DB, Wolford JK, Popovich BW.
    Am J Hum Genet; 1997 Jan 01; 60(1):160-5. PubMed ID: 8981959
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  • 15. Detection of new paternal dystrophin gene mutations in isolated cases of dystrophinopathy in females.
    Pegoraro E, Schimke RN, Arahata K, Hayashi Y, Stern H, Marks H, Glasberg MR, Carroll JE, Taber JW, Wessel HB.
    Am J Hum Genet; 1994 Jun 01; 54(6):989-1003. PubMed ID: 8198142
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  • 16. 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 01; 46(4):672-81. PubMed ID: 2180286
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  • 17. 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 Apr 01; 3(2):133-40. PubMed ID: 8199594
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  • 18. Very small dystrophin molecule in a family with a mild form of Becker dystrophy.
    Morandi L, Mora M, Bernasconi P, Mantegazza R, Gebbia M, Balestrini MR, Cornelio F.
    Neuromuscul Disord; 1993 Jan 01; 3(1):65-70. PubMed ID: 8329891
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  • 19. Dystrophin abnormality in progressive muscular dystrophy--a review article.
    Arahata K.
    Acta Paediatr Jpn; 1991 Apr 01; 33(2):216-21. PubMed ID: 1957648
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  • 20. Detection of carriers of deletions in the dystrophin gene in Bulgarian DMD-BMD families.
    Bronzova J, Todorova A, Kalaydjieva L.
    Hum Genet; 1994 Feb 01; 93(2):170-4. PubMed ID: 8112741
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