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Journal Abstract Search

192 related items for PubMed ID: 8940277

  • 1. Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb.
    Toda T, Miyake M, Kobayashi K, Mizuno K, Saito K, Osawa M, Nakamura Y, Kanazawa I, Nakagome Y, Tokunaga K, Nakahori Y.
    Am J Hum Genet; 1996 Dec; 59(6):1313-20. PubMed ID: 8940277
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  • 4. [Molecular genetics and merosin abnormality in Fukuyama-type congenital muscular dystrophy (FCMD)].
    Toda T, Kobayashi K.
    Nihon Rinsho; 1997 Dec; 55(12):3169-75. PubMed ID: 9436430
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  • 5. Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: evidence for strong linkage disequilibrium.
    Toda T, Ikegawa S, Okui K, Kondo E, Saito K, Fukuyama Y, Yoshioka M, Kumagai T, Suzumori K, Kanazawa I.
    Am J Hum Genet; 1994 Nov; 55(5):946-50. PubMed ID: 7977357
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  • 7. Age and origin of the FCMD 3'-untranslated-region retrotransposal insertion mutation causing Fukuyama-type congenital muscular dystrophy in the Japanese population.
    Colombo R, Bignamini AA, Carobene A, Sasaki J, Tachikawa M, Kobayashi K, Toda T.
    Hum Genet; 2000 Dec; 107(6):559-67. PubMed ID: 11153909
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  • 9. [Recent progress, genetic diagnosis and its problem on congenital muscular dystrophies (Fukuyama and non-Fukuyama types)].
    Toda T.
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1419-21. PubMed ID: 8752416
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  • 11. Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33.
    Toda T, Segawa M, Nomura Y, Nonaka I, Masuda K, Ishihara T, Sakai M, Tomita I, Origuchi Y, Suzuki M [corrected to Sakai M].
    Nat Genet; 1993 Nov; 5(3):283-6. PubMed ID: 8275093
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  • 12. An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy.
    Kobayashi K, Nakahori Y, Miyake M, Matsumura K, Kondo-Iida E, Nomura Y, Segawa M, Yoshioka M, Saito K, Osawa M, Hamano K, Sakakihara Y, Nonaka I, Nakagome Y, Kanazawa I, Nakamura Y, Tokunaga K, Toda T.
    Nature; 1998 Jul 23; 394(6691):388-92. PubMed ID: 9690476
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  • 15. Haplotype-phenotype correlation in Fukuyama congenital muscular dystrophy.
    Saito K, Osawa M, Wang ZP, Ikeya K, Fukuyama Y, Kondo-Iida E, Toda T, Ohashi H, Kurosawa K, Wakai S, Kaneko K.
    Am J Med Genet; 2000 May 29; 92(3):184-90. PubMed ID: 10817652
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  • 16. Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome.
    Toda T, Yoshioka M, Nakahori Y, Kanazawa I, Nakamura Y, Nakagome Y.
    Ann Neurol; 1995 Jan 29; 37(1):99-101. PubMed ID: 7818265
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  • 17. Fukuyama-type congenital muscular dystrophy: the first human disease to be caused by an ancient retrotransposal integration.
    Toda T, Kobayashi K.
    J Mol Med (Berl); 1999 Dec 29; 77(12):816-23. PubMed ID: 10682317
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  • 19. [Hint and luck for identification of a gene for Fukuyama muscular dystrophy, fukutin].
    Toda T.
    Rinsho Shinkeigaku; 2007 Nov 29; 47(11):743-8. PubMed ID: 18210789
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