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Journal Abstract Search

184 related items for PubMed ID: 8808603

  • 1.
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  • 2. Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophy.
    Illarioshkin SN, Ivanova-Smolenskaya IA, Tanaka H, Vereshchagin NV, Markova ED, Poleshchuk VV, Lozhnikova SM, Sukhorukov VS, Limborska SA, Slominsky PA, Bulayeva KB, Tsuji S.
    Brain; 1996 Dec; 119 ( Pt 6)():1895-909. PubMed ID: 9009996
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  • 3. Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2p.
    Bashir R, Keers S, Strachan T, Passos-Bueno R, Zatz M, Weissenbach J, Le Paslier D, Meisler M, Bushby K.
    Genomics; 1996 Apr 01; 33(1):46-52. PubMed ID: 8617508
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  • 5. A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.
    Weiler T, Greenberg CR, Zelinski T, Nylen E, Coghlan G, Crumley MJ, Fujiwara TM, Morgan K, Wrogemann K.
    Am J Hum Genet; 1998 Jul 01; 63(1):140-7. PubMed ID: 9634523
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  • 6. [Mapping of the gene for autosomal-recessive progressive muscular dystrophy in an isolate from a highland region of Dagestan to chromosome 2-13].
    Illarioshkin SN, Ivanova-Smolenskaia IA, Dimborskaia SA, Poleshchuk VV, Markova ED, Slominskiĭ PA, Bulaeva KB, Tsudzi Sh.
    Genetika; 1997 Nov 01; 33(11):1551-8. PubMed ID: 9480219
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  • 10. Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s).
    Weiler T, Bashir R, Anderson LV, Davison K, Moss JA, Britton S, Nylen E, Keers S, Vafiadaki E, Greenberg CR, Bushby CR, Wrogemann K.
    Hum Mol Genet; 1999 May 01; 8(5):871-7. PubMed ID: 10196377
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  • 13. Genetic fine mapping of the Miyoshi myopathy locus and exclusion of eight candidate genes.
    Bejaoui K, Liu J, McKenna-Yasek D, Le Paslier D, Bossie K, Gilligan DM, Brown RH.
    Neurogenetics; 1998 Mar 01; 1(3):189-96. PubMed ID: 10737122
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  • 15. Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy.
    Speer MC, Gilchrist JM, Chutkow JG, McMichael R, Westbrook CA, Stajich JM, Jorgenson EM, Gaskell PC, Rosi BL, Ramesar R.
    Am J Hum Genet; 1995 Dec 01; 57(6):1371-6. PubMed ID: 8533766
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  • 16. Limb girdle muscular dystrophy in Manitoba Hutterites does not map to any of the known LGMD loci.
    Weiler T, Greenberg CR, Nylen E, Morgan K, Fujiwara TM, Crumley MJ, Zelinski T, Halliday W, Nickel B, Triggs-Raine B, Wrogemann K.
    Am J Med Genet; 1997 Oct 31; 72(3):363-8. PubMed ID: 9332671
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  • 17. Limb-girdle muscular dystrophy: a follow-up study of 79 patients.
    Mahjneh I, Bushby K, Pizzi A, Bashir R, Marconi G.
    Acta Neurol Scand; 1996 Sep 31; 94(3):177-89. PubMed ID: 8899051
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  • 18. Dysferlin protein analysis in limb-girdle muscular dystrophies.
    Vainzof M, Anderson LV, McNally EM, Davis DB, Faulkner G, Valle G, Moreira ES, Pavanello RC, Passos-Bueno MR, Zatz M.
    J Mol Neurosci; 2001 Aug 31; 17(1):71-80. PubMed ID: 11665864
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