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Journal Abstract Search

401 related items for PubMed ID: 15841391

  • 1. Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA).
    Gatta V, Scarciolla O, Gaspari AR, Palka C, De Angelis MV, Di Muzio A, Guanciali-Franchi P, Calabrese G, Uncini A, Stuppia L.
    Hum Genet; 2005 Jun; 117(1):92-8. PubMed ID: 15841391
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  • 4. [Combining approach with multiplex PCR and MLPA to detect deletion and duplication in DMD patients, carriers, and prenatal diagnosis].
    Li H, Ding J, Wang W, Chen Y, Lu W, Shao H, Wu BL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):318-22. PubMed ID: 19504448
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  • 5. [Detection of genomic duplications and deletions of the DMD gene in affected males and female carriers by using mutiplex ligation-dependent probe amplification].
    Shen BC, Zhang C, Sun XF, Zhang HM, Li SY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):460-3. PubMed ID: 17680544
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  • 7. 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; 15(12):893-9. PubMed ID: 21815800
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  • 8. Improved detection of deletions and duplications in the DMD gene using the multiplex ligation-dependent probe amplification (MLPA) method.
    Sansović I, Barišić I, Dumić K.
    Biochem Genet; 2013 Apr; 51(3-4):189-201. PubMed ID: 23224783
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  • 9. 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 Apr; 59(6):803-9. PubMed ID: 22234189
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  • 11. Carrier detection in Duchenne muscular dystrophy using molecular methods.
    Sakthivel Murugan SM, Arthi C, Thilothammal N, Lakshmi BR.
    Indian J Med Res; 2013 Jun; 137(6):1102-10. PubMed ID: 23852291
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  • 13. 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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  • 15. 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; 27(3):274-80. PubMed ID: 22379338
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  • 16. [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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  • 17. [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 25; 48(3):161-4. PubMed ID: 23849935
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