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Journal Abstract Search

750 related items for PubMed ID: 24213305

  • 1.
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  • 2. 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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  • 3. 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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  • 6. [Genetic analysis and prenatal diagnosis of Duchenne or Becker muscular dystrophy].
    Zhao W, Jiang N, Li S, Li JS, Miao Y, Liang SY, Yu DY.
    Zhonghua Fu Chan Ke Za Zhi; 2019 Apr 25; 54(4):226-231. PubMed ID: 31006187
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  • 9. 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 25; 19(2):108-12. PubMed ID: 19084397
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  • 11. Dystrophin gene mutation analysis in Iranian males and females using multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification methods.
    Khordadpoor-Deilamani F, Akbari MT, Nafissi S, Zamani G.
    Genet Test Mol Biomarkers; 2011 Dec 25; 15(12):893-9. PubMed ID: 21815800
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  • 12. Genetic analysis of dystrophin gene for affected male and female carriers with Duchenne/Becker muscular dystrophy in Korea.
    Lee BL, Nam SH, Lee JH, Ki CS, Lee M, Lee J.
    J Korean Med Sci; 2012 Mar 25; 27(3):274-80. PubMed ID: 22379338
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  • 14. Molecular Analysis-Based Genetic Characterization of a Cohort of Patients with Duchenne and Becker Muscular Dystrophy in Eastern China.
    Zhao HH, Sun XP, Shi MC, Yi YX, Cheng H, Wang XX, Xu QC, Ma HM, Wu HQ, Jin QW, Niu Q.
    Chin Med J (Engl); 2018 Apr 05; 131(7):770-775. PubMed ID: 29578119
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  • 15. Molecular analysis of the dystrophin gene in 407 Chinese patients with Duchenne/Becker muscular dystrophy by the combination of multiplex ligation-dependent probe amplification and Sanger sequencing.
    Chen WJ, Lin QF, Zhang QJ, He J, Liu XY, Lin MT, Murong SX, Liou CW, Wang N.
    Clin Chim Acta; 2013 Aug 23; 423():35-8. PubMed ID: 23588064
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  • 16. [Mutation analysis and prenatal diagnosis of families affected with Duchenne and Becker muscular dystrophy].
    Wang WJ, Zhu HY, Zhu RF, Yang Y, Zhu XY, Duan HL, Zhang Y, Wu X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb 23; 30(1):45-8. PubMed ID: 23450478
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  • 18. Improved molecular diagnosis of dystrophin gene mutations using the multiplex ligation-dependent probe amplification method.
    Schwartz M, Dunø M.
    Genet Test; 2004 Feb 23; 8(4):361-7. PubMed ID: 15684864
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  • 19. Genetic analysis of the dystrophin gene in children with Duchenne and Becker muscular dystrophies.
    Zhong J, Xu T, Chen G, Liao H, Zhang J, Lan D.
    Muscle Nerve; 2017 Jul 23; 56(1):117-121. PubMed ID: 27750387
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  • 20. [Clinical value of MLPA in the prenatal gene diagnosis of Duchenne muscular dystrophy].
    Li Q, Li SY, Zhang HM, He WZ, Ma XY, Wang XM, Xian JJ, Sun XF, Chen DJ, Yu YH.
    Zhonghua Fu Chan Ke Za Zhi; 2013 Mar 23; 48(3):161-4. PubMed ID: 23849935
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