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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

239 related items for PubMed ID: 23223008

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  • 9. Intravenous infusion of an antisense oligonucleotide results in exon skipping in muscle dystrophin mRNA of Duchenne muscular dystrophy.
    Takeshima Y, Yagi M, Wada H, Ishibashi K, Nishiyama A, Kakumoto M, Sakaeda T, Saura R, Okumura K, Matsuo M.
    Pediatr Res; 2006 May; 59(5):690-4. PubMed ID: 16627883
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  • 15. Point mutations in the dystrophin gene: evidence for frequent use of cryptic splice sites as a result of splicing defects.
    Tuffery-Giraud S, Chambert S, Demaille J, Claustres M.
    Hum Mutat; 1999 May; 14(5):359-68. PubMed ID: 10533061
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  • 17. Tandem duplications of two separate fragments of the dystrophin gene in a patient with Duchenne muscular dystrophy.
    Zhang Z, Takeshima Y, Awano H, Nishiyama A, Okizuka Y, Yagi M, Matsuo M.
    J Hum Genet; 2008 May; 53(3):215-219. PubMed ID: 18160999
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  • 18. Use of multiplex ligation-dependent probe amplification (MLPA) for Duchenne muscular dystrophy (DMD) gene mutation analysis.
    Murugan S, Chandramohan A, Lakshmi BR.
    Indian J Med Res; 2010 Sep; 132():303-11. PubMed ID: 20847377
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  • 19. Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy.
    Giliberto F, Ferreiro V, Dalamon V, Szijan I.
    Neurol Res; 2004 Jan; 26(1):83-7. PubMed ID: 14977063
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