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Journal Abstract Search

133 related items for PubMed ID: 11402447

  • 1. [Intron 44 is not the most unstable intron in the "central deletion hot spot" of dystrophin gene].
    Pan S, Xie Y, Zhang C, Liu Z, Chen G, Lu X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Jun; 18(3):191-4. PubMed ID: 11402447
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  • 2. Mutation analysis in Duchenne and Becker muscular dystrophy patients from Bulgaria shows a peculiar distribution of breakpoints by intron.
    Todoroya A, Bronzova J, Miorin M, Rosa M, Kremensky I, Danieli GA.
    Am J Med Genet; 1996 Oct 02; 65(1):40-3. PubMed ID: 8914739
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  • 3. [Studying dystrophin gene deletion in the northeast of China and applicating].
    Lu Y, Jin CL, Lin CK, Wu YY, Liu LY, Sun KL.
    Yi Chuan Xue Bao; 2004 May 02; 31(5):449-53. PubMed ID: 15478603
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  • 4. Comparative study on deletions of the dystrophin gene in three Asian populations.
    Lai PS, Takeshima Y, Adachi K, Van Tran K, Nguyen HT, Low PS, Matsuo M.
    J Hum Genet; 2002 May 02; 47(10):552-5. PubMed ID: 12376747
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  • 7. Patterns of deletions and the distribution of breakpoints in the dystrophin gene in Czech patients with Duchenne and Becker muscular dystrophy (statistical comparison with results from several other countries).
    Hrdlicka I, Zadina J, Krejcí R, Srbová A, Kucerová M.
    Folia Biol (Praha); 2001 May 02; 47(3):81-7. PubMed ID: 11409318
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  • 10. [Cloning and sequencing of the junction fragment of dystrophin gene with exons 3 to 5 deletion].
    Zhong M, Pan SY, Lu BX, Jiang L, Li W.
    Nan Fang Yi Ke Da Xue Xue Bao; 2006 Jun 02; 26(6):757-9. PubMed ID: 16793593
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  • 12. Analysis of dystrophin gene deletions in patients from the Mexican population with Duchenne/Becker muscular dystrophy.
    Coral-Vázquez R, Arenas D, Cisneros B, Peñaloza L, Kofman S, Salamanca F, Montañez C.
    Arch Med Res; 1993 Jun 02; 24(1):1-6. PubMed ID: 8292871
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  • 13. Deletion screening of the Duchenne/Becker muscular dystrophy gene in Croatian population.
    Sertić J, Barisić N, Sostarko M, Brzović Z, Stavljenić-Rukavina A.
    Coll Antropol; 1997 Jun 02; 21(1):151-6. PubMed ID: 9225508
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  • 14. [Cloning and sequencing of junction fragment with exon 51 deletion of Dystrophin gene].
    Pan SY, Zhang C, Liu ZL, Chen GJ, Lu XL.
    Yi Chuan Xue Bao; 2002 Feb 02; 29(2):105-10. PubMed ID: 11901990
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  • 17. Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients.
    Dinçer P, Topaloğlu H, Ayter S, Ozgüç M, Taşdemir HA, Renda Y.
    Brain Dev; 1996 Feb 02; 18(2):91-4. PubMed ID: 8733896
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  • 18. Newly recognized exons induced by a splicing abnormality from an intronic mutation of the dystrophin gene resulting in Duchenne muscular dystrophy. Mutations in brief no. 213. Online.
    Ikezawa M, Nishino I, Goto Y, Miike T, Nonaka I.
    Hum Mutat; 1999 Feb 02; 13(2):170. PubMed ID: 10094556
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  • 19. Additional dystrophin fragment in Becker muscular dystrophy may result from proteolytic cleavage at deletion junctions.
    Beggs AH, Hoffman EP, Kunkel LM.
    Am J Med Genet; 1992 Oct 01; 44(3):378-81. PubMed ID: 1488990
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  • 20. Molecular deletion patterns in Duchenne and Becker muscular dystrophy patients from KwaZulu Natal.
    Hallwirth Pillay KD, Bill PL, Madurai S, Mubaiwa L, Rapiti P.
    J Neurol Sci; 2007 Jan 15; 252(1):1-3. PubMed ID: 17141273
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