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PUBMED FOR HANDHELDS

Journal Abstract Search

92 related items for PubMed ID: 7951237

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  • 3. 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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  • 4. Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?
    Vainzof M, Takata RI, Passos-Bueno MR, Pavanello RC, Zatz M.
    Hum Mol Genet; 1993 Jan; 2(1):39-42. PubMed ID: 8490621
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  • 5. Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophy.
    Winnard AV, Klein CJ, Coovert DD, Prior T, Papp A, Snyder P, Bulman DE, Ray PN, McAndrew P, King W.
    Hum Mol Genet; 1993 Jun; 2(6):737-44. PubMed ID: 8353493
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  • 10. Deletions in the 5' region of dystrophin and resulting phenotypes.
    Muntoni F, Gobbi P, Sewry C, Sherratt T, Taylor J, Sandhu SK, Abbs S, Roberts R, Hodgson SV, Bobrow M.
    J Med Genet; 1994 Nov; 31(11):843-7. PubMed ID: 7853367
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  • 13. Southern blot and PCR analyses of dystrophin gene deletions in Japanese patients with Duchenne muscular dystrophy.
    Nakajima T, Matsuo M, Nakamura H, Fujiwara Y.
    Kobe J Med Sci; 1991 Feb; 37(1):21-33. PubMed ID: 1921260
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  • 17. Splicing mutations in DMD/BMD detected by RT-PCR/PTT: detection of a 19AA insertion in the cysteine rich domain of dystrophin compatible with BMD.
    Roest PA, Bout M, van der Tuijn AC, Ginjaar IB, Bakker E, Hogervorst FB, van Ommen GJ, den Dunnen JT.
    J Med Genet; 1996 Nov; 33(11):935-9. PubMed ID: 8950674
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  • 20. 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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