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Journal Abstract Search

235 related items for PubMed ID: 16553208

  • 1. 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; 33(3):206-12. PubMed ID: 16553208
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  • 2. [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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  • 3. [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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  • 4. Prenatal diagnosis of Duchenne/Becker muscular dystrophy by short tandem repeat segregation analysis in Argentine families.
    Giliberto F, Ferreiro V, Massot F, Ferrer M, Francipane L, Szijan I.
    Muscle Nerve; 2011 Apr 07; 43(4):510-7. PubMed ID: 21305566
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  • 6. DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients.
    Hofstra RM, Mulder IM, Vossen R, de Koning-Gans PA, Kraak M, Ginjaar IB, van der Hout AH, Bakker E, Buys CH, van Ommen GJ, van Essen AJ, den Dunnen JT.
    Hum Mutat; 2004 Jan 07; 23(1):57-66. PubMed ID: 14695533
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  • 8. [Carrier detection of Duchenne/Becker muscular dystrophy by analysis of STRs loci linked to the gene of dystrophin in Venezuelan families].
    Delgado-Luengo WN, Borjas-Fuentes L, Zabala-Fernández W, Fernández-Salgado E, Solís-Añez E, Chávez C, Martínez-Basalo C, González-Ferrer S, Rojas-Atencio A, Morales-Machin A, Peña J, Pineda-Bernal L, González R, Miranda LE, Delgado-Luengo J, Hernández ML, Chacín JA, Quintero M.
    Invest Clin; 2002 Dec 07; 43(4):239-54. PubMed ID: 12520997
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  • 9. Deletion analysis of the dystrophin gene in Duchenne and Becker muscular dystrophy patients: use in carrier diagnosis.
    Kumari D, Mital A, Gupta M, Goyle S.
    Neurol India; 2003 Jun 07; 51(2):223-6. PubMed ID: 14571009
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  • 11. [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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  • 17. Paternal inheritance or a de novo mutation in a Duchenne Muscular Dystrophy pedigree from South India.
    Purushottam M, Murthy AR, Shubha GN, Gayathri N, Nalini A.
    J Neurol Sci; 2008 May 15; 268(1-2):179-82. PubMed ID: 18031759
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  • 18. Comparison of serum creatine kinase estimation with short tandem repeats based linkage analysis in carriers and affected children of Duchenne muscular dystrophy.
    Hashim R, Shaheen S, Ahmad S, Sattar A, Khan FA.
    J Ayub Med Coll Abbottabad; 2011 May 15; 23(1):125-8. PubMed ID: 22830166
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  • 19. Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene.
    Deburgrave N, Daoud F, Llense S, Barbot JC, Récan D, Peccate C, Burghes AH, Béroud C, Garcia L, Kaplan JC, Chelly J, Leturcq F.
    Hum Mutat; 2007 Feb 15; 28(2):183-95. PubMed ID: 17041906
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