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PUBMED FOR HANDHELDS

Journal Abstract Search

700 related items for PubMed ID: 14695533

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  • 3. Rapid and cost effective detection of small mutations in the DMD gene by high resolution melting curve analysis.
    Almomani R, van der Stoep N, Bakker E, den Dunnen JT, Breuning MH, Ginjaar IB.
    Neuromuscul Disord; 2009 Jun; 19(6):383-90. PubMed ID: 19409785
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  • 10. [Identification of disease-causing point mutations in DMD patients' dystrophin gene without large deletions/duplications].
    Shen BC, Zhang C, Chen SL, Sun XF, Li SY, Yao XL, Wang SH, Lu XL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Aug; 23(4):392-6. PubMed ID: 16883524
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  • 11. Simultaneous mutation scanning for gross deletions, duplications and point mutations in the DMD gene.
    Ashton EJ, Yau SC, Deans ZC, Abbs SJ.
    Eur J Hum Genet; 2008 Jan; 16(1):53-61. PubMed ID: 17726484
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  • 13. [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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  • 14. [From gene to disease; the dystrophin gene involved in Duchenne and Becker muscular dystrophy].
    den Dunnen JT, de Visser M, Bakker E.
    Ned Tijdschr Geneeskd; 2002 Feb 23; 146(8):364-7. PubMed ID: 11887623
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  • 17. [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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  • 18. Genetic polymorphism in muscle biopsies of Duchenne and Becker muscular dystrophy patients.
    Anand A, Prabhakar S, Kaul D.
    Neurol India; 1999 Sep 07; 47(3):218-23. PubMed ID: 10514583
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  • 20. [Application of PCR technique in genetic diagnosis of Duchenne/Becker muscular dystrophy].
    Liu YM, Feng ZC, Fang ZW.
    Di Yi Jun Yi Da Xue Xue Bao; 2002 Aug 07; 22(8):731-3. PubMed ID: 12376264
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