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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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  • 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 Feb; 186(4):349-53. PubMed ID: 1301222
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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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  • 9. [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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  • 10. 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. 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 Feb 15; 26 Suppl 1():172-4. PubMed ID: 8629100
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  • 18. Follow-up of three patients with a large in-frame deletion of exons 45-55 in the Duchenne muscular dystrophy (DMD) gene.
    Nakamura A, Yoshida K, Fukushima K, Ueda H, Urasawa N, Koyama J, Yazaki Y, Yazaki M, Sakai T, Haruta S, Takeda S, Ikeda S.
    J Clin Neurosci; 2008 Jul 15; 15(7):757-63. PubMed ID: 18261911
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  • 20. 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 15; 12(5):353-6. PubMed ID: 16608904
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