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PUBMED FOR HANDHELDS

Journal Abstract Search


279 related items for PubMed ID: 8411068

  • 21. The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. II. Correlation of phenotype with genetic and protein abnormalities.
    Bushby KM, Gardner-Medwin D, Nicholson LV, Johnson MA, Haggerty ID, Cleghorn NJ, Harris JB, Bhattacharya SS.
    J Neurol; 1993 Feb; 240(2):105-12. PubMed ID: 8437017
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  • 22. Very mild muscular dystrophy associated with the deletion of 46% of dystrophin.
    England SB, Nicholson LV, Johnson MA, Forrest SM, Love DR, Zubrzycka-Gaarn EE, Bulman DE, Harris JB, Davies KE.
    Nature; 1990 Jan 11; 343(6254):180-2. PubMed ID: 2404210
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  • 23. Detection of DMD gene deletions in Thai children patients.
    Kamolsilp M, Paditaporn R, Noonai A, Wasant P.
    Southeast Asian J Trop Med Public Health; 1995 Jan 11; 26 Suppl 1():172-4. PubMed ID: 8629100
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  • 31. Intragenic deletions in the dystrophin gene in 211 Pakistani Duchenne muscular dystrophy patients.
    Hassan MJ, Mahmood S, Ali G, Bibi N, Waheed I, Rafiq MA, Ansar M, Ahmad W.
    Pediatr Int; 2008 Apr 11; 50(2):162-6. PubMed ID: 18353051
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  • 33. Is dystrophin always altered in Becker muscular dystrophy patients?
    Vainzof M, Passos-Bueno MR, Pavanello RC, Zatz M.
    J Neurol Sci; 1995 Jul 11; 131(1):99-104. PubMed ID: 7561956
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  • 35. MLPA based detection of mutations in the dystrophin gene of 180 Polish families with Duchenne/Becker muscular dystrophy.
    Zimowski JG, Massalska D, Holding M, Jadczak S, Fidziańska E, Lusakowska A, Kostera-Pruszczyk A, Kamińska A, Zaremba J.
    Neurol Neurochir Pol; 2014 Jul 11; 48(6):416-22. PubMed ID: 25482253
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