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Journal Abstract Search

343 related items for PubMed ID: 8411723

  • 1. [Molecular genetics of Duchenne/Becker muscular dystrophy].
    Saito K, Ikeya K, Kondo E, Yamauchi A, Komine S, Fukuyama Y.
    Nihon Rinsho; 1993 Sep; 51(9):2420-7. PubMed ID: 8411723
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  • 2. [Molecular pathology of Duchenne and Becker muscular dystrophy].
    Gilgenkrantz H, Chelly J, Récan D, Chafey P, Kaplan JC.
    C R Seances Soc Biol Fil; 1992 Sep; 186(4):349-53. PubMed ID: 1301222
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  • 3. [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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  • 4. Dystrophin as a diagnostic marker in Duchenne and Becker muscular dystrophy. Correlation of immunofluorescence and western blot.
    Voit T, Stuettgen P, Cremer M, Goebel HH.
    Neuropediatrics; 1991 Aug; 22(3):152-62. PubMed ID: 1944822
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  • 5. 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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  • 6. [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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  • 8. Re-evaluation of reading frame-shift hypothesis in Duchenne and Becker muscular dystrophy.
    Pandey GS, Kesari A, Mukherjee M, Mittal RD, Mittal B.
    Neurol India; 2003 Sep 23; 51(3):367-9. PubMed ID: 14652441
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  • 9. Duchenne and Becker muscular dystrophy: from gene diagnosis to molecular therapy.
    Matsuo M.
    IUBMB Life; 2002 Mar 23; 53(3):147-52. PubMed ID: 12102170
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  • 10. Large in-frame deletions of the rod-shaped domain of the dystrophin gene resulting in severe phenotype.
    Nevo Y, Muntoni F, Sewry C, Legum C, Kutai M, Harel S, Dubowitz V.
    Isr Med Assoc J; 2003 Feb 23; 5(2):94-7. PubMed ID: 12674656
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  • 11. Identification of three novel mutations in the dystrophin gene detected by the heteroduplex/SSCA screening procedure. Mutations in brief no. 222. Online.
    Dubourg C, Odent S, Fergelot P, Le Gall JY, David V, Blayau M.
    Hum Mutat; 1999 Feb 23; 13(2):173. PubMed ID: 10094565
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  • 12. 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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  • 13. [Correlation between genotypes and phenotypes in pseudohypertrophic muscular dystrophy].
    Feng SW, Liang YY, Cao JQ, Song XM, Zhang C.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Dec 23; 29(6):653-7. PubMed ID: 23225043
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  • 15. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients.
    Shomrat R, Gluck E, Legum C, Shiloh Y.
    Am J Med Genet; 1994 Feb 15; 49(4):369-73. PubMed ID: 8160727
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  • 16. Becker muscular dystrophy: detection of unusual disease courses by combined approach to dystrophin analysis.
    Gold R, Kress W, Meurers B, Meng G, Reichmann H, Müller CR.
    Muscle Nerve; 1992 Feb 15; 15(2):214-8. PubMed ID: 1549142
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  • 17. Proximal dystrophin gene deletions and protein alterations in becker muscular dystrophy.
    Novaković I, Bojić D, Todorović S, Apostolski S, Luković L, Stefanović D, Milasin J.
    Ann N Y Acad Sci; 2005 Jun 15; 1048():406-10. PubMed ID: 16154963
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  • 18. [Detection of extensive deletions and duplications in the dystrophin gene].
    Fajkusová L, Kuhrová V, Hájek J, Fajkus J.
    Cas Lek Cesk; 1997 Mar 12; 136(5):148-50. PubMed ID: 9221188
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