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Journal Abstract Search

266 related items for PubMed ID: 12674656

  • 1. 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; 5(2):94-7. PubMed ID: 12674656
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  • 2. Dystrophin expression in Duchenne patients with "in-frame" gene deletions.
    Nicholson LV, Bushby KM, Johnson MA, Gardner-Medwin D, Ginjaar IB.
    Neuropediatrics; 1993 Apr; 24(2):93-7. PubMed ID: 8327067
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  • 3. [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 Apr; 186(4):349-53. PubMed ID: 1301222
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  • 4. 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; 1048():406-10. PubMed ID: 16154963
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  • 5. Amplification of selected exons by polymerase chain reaction enables determination of the translational reading frame of dystrophin mRNA resulting from deletion mutations.
    Kitoh Y, Matsuo M, Nishio H, Nakamura H.
    Kobe J Med Sci; 1994 Apr; 40(2):39-48. PubMed ID: 7823533
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  • 6. [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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  • 9. [Molecular genetics and problems found in genetic diagnosis of Duchenne Becker muscular dystrophy].
    Takeshima Y, Matsuo M.
    Nihon Rinsho; 1997 Dec 12; 55(12):3120-5. PubMed ID: 9436421
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  • 11. 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 12; 51(2):223-6. PubMed ID: 14571009
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  • 16. Detection of DMD gene deletions in Thai children patients.
    Kamolsilp M, Paditaporn R, Noonai A, Wasant P.
    Southeast Asian J Trop Med Public Health; 1995 Jun 12; 26 Suppl 1():172-4. PubMed ID: 8629100
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  • 19. [Family study allows more optimistic prognosis and genetic counselling in a child with a deletion of exons 50-51 of the dystrophin gene].
    Lesca G, Testard H, Streichenberger N, Pelissier JF, Lestra C, Burel E, Jonveaux P, Michel-Calemard L.
    Arch Pediatr; 2007 Mar 12; 14(3):262-5. PubMed ID: 17258443
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