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Journal Abstract Search

346 related items for PubMed ID: 17680544

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  • 3. [Identification of deletion/duplication mutations in DMD gene by multiple ligation probe amplification and denaturing high-performance liquid chromatography].
    Shen BC, Zhang C, Sun XF, Li SY.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2007 Feb; 29(1):83-6. PubMed ID: 17380674
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  • 4. Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families - detection of carrier status in symptomatic and asymptomatic female relatives.
    Pikó H, Vancsó V, Nagy B, Bán Z, Herczegfalvi A, Karcagi V.
    Neuromuscul Disord; 2009 Feb; 19(2):108-12. PubMed ID: 19084397
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  • 5. Detecting exon deletions and duplications of the DMD gene using Multiplex Ligation-dependent Probe Amplification (MLPA).
    Lai KK, Lo IF, Tong TM, Cheng LY, Lam ST.
    Clin Biochem; 2006 Apr; 39(4):367-72. PubMed ID: 16413013
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  • 7. Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization.
    del Gaudio D, Yang Y, Boggs BA, Schmitt ES, Lee JA, Sahoo T, Pham HT, Wiszniewska J, Chinault AC, Beaudet AL, Eng CM.
    Hum Mutat; 2008 Sep; 29(9):1100-7. PubMed ID: 18752307
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  • 8. MLPA analysis/complete sequencing of the DMD gene in a group of Bulgarian Duchenne/Becker muscular dystrophy patients.
    Todorova A, Todorov T, Georgieva B, Lukova M, Guergueltcheva V, Kremensky I, Mitev V.
    Neuromuscul Disord; 2008 Aug; 18(8):667-70. PubMed ID: 18653336
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  • 12. Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene.
    Deburgrave N, Daoud F, Llense S, Barbot JC, Récan D, Peccate C, Burghes AH, Béroud C, Garcia L, Kaplan JC, Chelly J, Leturcq F.
    Hum Mutat; 2007 Feb; 28(2):183-95. PubMed ID: 17041906
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  • 14. 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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  • 18. 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 Sep; 48(6):416-22. PubMed ID: 25482253
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  • 19. Identification of deletions and duplications in the Duchenne muscular dystrophy gene and female carrier status in western India using combined methods of multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification.
    Dastur RS, Kachwala MY, Khadilkar SV, Hegde MR, Gaitonde PS.
    Neurol India; 2011 Sep; 59(6):803-9. PubMed ID: 22234189
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