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Journal Abstract Search

445 related items for PubMed ID: 27750387

  • 1. 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; 56(1):117-121. PubMed ID: 27750387
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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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  • 6. 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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  • 8. Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations.
    Okubo M, Minami N, Goto K, Goto Y, Noguchi S, Mitsuhashi S, Nishino I.
    J Hum Genet; 2016 Jun 05; 61(6):483-9. PubMed ID: 26911353
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  • 9. 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 05; 27(3):274-80. PubMed ID: 22379338
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  • 11. Multiplex Ligation-Dependent Probe Amplification in X-linked Recessive Muscular Dystrophy in Korean Subjects.
    Suh MR, Lee KA, Kim EY, Jung J, Choi WA, Kang SW.
    Yonsei Med J; 2017 May 05; 58(3):613-618. PubMed ID: 28332368
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  • 13. Evaluation of point mutations in dystrophin gene in Iranian Duchenne and Becker muscular dystrophy patients: introducing three novel variants.
    Haghshenas M, Akbari MT, Karizi SZ, Deilamani FK, Nafissi S, Salehi Z.
    J Genet; 2016 Jun 05; 95(2):325-9. PubMed ID: 27350676
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  • 14. A splicing mutation in the DMD gene detected by next-generation sequencing and confirmed by mRNA and protein analysis.
    Roucher Boulez F, Menassa R, Streichenberger N, Manel V, Mallet-Motak D, Morel Y, Michel-Calemard L.
    Clin Chim Acta; 2015 Aug 25; 448():146-9. PubMed ID: 26148721
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  • 15. Whole dystrophin gene analysis by next-generation sequencing: a comprehensive genetic diagnosis of Duchenne and Becker muscular dystrophy.
    Wang Y, Yang Y, Liu J, Chen XC, Liu X, Wang CZ, He XY.
    Mol Genet Genomics; 2014 Oct 25; 289(5):1013-21. PubMed ID: 24770780
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  • 16. Analysis of dystrophin gene in Iranian Duchenne and Becker muscular dystrophies patients and identification of a novel mutation.
    Zamani GR, Karami F, Mehdizadeh M, Movafagh A, Nilipour Y, Zamani M.
    Neurol Sci; 2015 Nov 25; 36(11):2011-7. PubMed ID: 26081009
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  • 17. Mutation spectrum analysis of Duchenne/Becker muscular dystrophy in 68 families in Kuwait: The era of personalized medicine.
    Mohammed F, Elshafey A, Al-Balool H, Alaboud H, Al Ben Ali M, Baqer A, Bastaki L.
    PLoS One; 2018 Nov 25; 13(5):e0197205. PubMed ID: 29847600
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  • 18. Genetic profile of Brazilian patients with dystrophinopathies.
    de Almeida PAD, Machado-Costa MC, Manzoli GN, Ferreira LS, Rodrigues MCS, Bueno LSM, Saute JAM, Pinto Vairo F, Matte US, Siebert M, Cossio SL, Macedo GS, Winckler PB, Becker MM, Magalhães LVB, Gonçalves MVM, Marrone CD, Nucci A, França MC.
    Clin Genet; 2017 Aug 25; 92(2):199-203. PubMed ID: 28116794
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  • 19. A De novo Mutation in Dystrophin Causing Muscular Dystrophy in a Female Patient.
    Yu H, Chen YC, Liu GL, Wu ZY.
    Chin Med J (Engl); 2017 Oct 05; 130(19):2273-2278. PubMed ID: 28937030
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  • 20. [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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