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Journal Abstract Search

206 related items for PubMed ID: 19862979

  • 1. [Mutation analysis and prenatal diagnosis of sporadic DMD/BMD families].
    Zhu HY, Li J, Yang Y, Wu X, Zhu XY, Zhu RF, Zhang Y, Duan HL, Hu YL.
    Zhonghua Yi Xue Za Zhi; 2009 Jul 07; 89(25):1753-6. PubMed ID: 19862979
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  • 2. [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 07; 26(3):318-22. PubMed ID: 19504448
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  • 3. [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 07; 30(1):45-8. PubMed ID: 23450478
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  • 4. Identify female carriers and de novo mutations in deletional Duchenne/Becker muscular dystrophy families.
    Zhu HY, Wu LQ, Liang DS, Pan Q, Xia JH.
    Yi Chuan Xue Bao; 2006 Mar 07; 33(3):206-12. PubMed ID: 16553208
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  • 6. 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 07; 132():303-11. PubMed ID: 20847377
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  • 7. 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 07; 19(2):108-12. PubMed ID: 19084397
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  • 9. Validation and comparison of two quantitative real-time PCR assays for direct detection of DMD/BMD carriers.
    Hayat Nosaeid M, Mahdian R, Jamali S, Maryami F, Babashah S, Maryami F, Karimipoor M, Zeinali S.
    Clin Biochem; 2009 Aug 07; 42(12):1291-9. PubMed ID: 19439162
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  • 13. Deletion and duplication screening in the DMD gene using MLPA.
    Lalic T, Vossen RH, Coffa J, Schouten JP, Guc-Scekic M, Radivojevic D, Djurisic M, Breuning MH, White SJ, den Dunnen JT.
    Eur J Hum Genet; 2005 Nov 07; 13(11):1231-4. PubMed ID: 16030524
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  • 18. [Carrier genetic diagnosis of intron and/or exon-deletion Duchenne muscular dystrophy by microsatellite analysis and quantitative polymerase chain reaction].
    Huang W, Zhang C, Xie YM, Chen SL, Zhang WX, Yao XL, Zeng Y, Lu XL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Feb 07; 24(1):72-5. PubMed ID: 17285549
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  • 19. Identification of female carriers for Duchenne and Becker muscular dystrophies using a FISH-based approach.
    Ligon AH, Kashork CD, Richards CS, Shaffer LG.
    Eur J Hum Genet; 2000 Apr 07; 8(4):293-8. PubMed ID: 10854113
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