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Journal Abstract Search

610 related items for PubMed ID: 20485447

  • 21.
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  • 22. 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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  • 25. 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; 51(2):223-6. PubMed ID: 14571009
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  • 27. [Molecular genetics and problems found in genetic diagnosis of Duchenne Becker muscular dystrophy].
    Takeshima Y, Matsuo M.
    Nihon Rinsho; 1997 Dec; 55(12):3120-5. PubMed ID: 9436421
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  • 30. 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; 8(4):293-8. PubMed ID: 10854113
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  • 32. Two alternative exons can result from activation of the cryptic splice acceptor site deep within intron 2 of the dystrophin gene in a patient with as yet asymptomatic dystrophinopathy.
    Yagi M, Takeshima Y, Wada H, Nakamura H, Matsuo M.
    Hum Genet; 2003 Feb; 112(2):164-70. PubMed ID: 12522557
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  • 34. DNA sequence analysis for structure/function and mutation studies in Becker muscular dystrophy.
    Hamed S, Sutherland-Smith A, Gorospe J, Kendrick-Jones J, Hoffman E.
    Clin Genet; 2005 Jul; 68(1):69-79. PubMed ID: 15952989
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  • 35. Genetic polymorphism in muscle biopsies of Duchenne and Becker muscular dystrophy patients.
    Anand A, Prabhakar S, Kaul D.
    Neurol India; 1999 Sep; 47(3):218-23. PubMed ID: 10514583
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  • 36. Two distinct mutations in a single dystrophin gene: identification of an altered splice-site as the primary Becker muscular dystrophy mutation.
    Wilton SD, Johnsen RD, Pedretti JR, Laing NG.
    Am J Med Genet; 1993 Jun 15; 46(5):563-9. PubMed ID: 8322822
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  • 37. MLPA based detection of mutations in the dystrophin gene of 180 Polish families with Duchenne/Becker muscular dystrophy.
    Zimowski JG, Massalska D, Holding M, Jadczak S, Fidziańska E, Lusakowska A, Kostera-Pruszczyk A, Kamińska A, Zaremba J.
    Neurol Neurochir Pol; 2014 Jun 15; 48(6):416-22. PubMed ID: 25482253
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  • 38. [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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  • 39. Deletion mutations in the dystrophin gene of Saudi patients with Duchenne and Becker muscular dystrophy.
    Al-Jumah M, Majumdar R, Al-Rajeh S, Chaves-Carballo E, Salih MM, Awada A, Al-Shahwan S, Al-Uthaim S.
    Saudi Med J; 2002 Dec 23; 23(12):1478-82. PubMed ID: 12518196
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  • 40. PGD for dystrophin gene deletions using fluorescence in situ hybridization.
    Malmgren H, White I, Johansson S, Levkov L, Iwarsson E, Fridström M, Blennow E.
    Mol Hum Reprod; 2006 May 23; 12(5):353-6. PubMed ID: 16608904
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