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Journal Abstract Search

150 related items for PubMed ID: 8320700

  • 1. Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian families.
    Passos-Bueno MR, Richard I, Vainzof M, Fougerousse F, Weissenbach J, Broux O, Cohen D, Akiyama J, Marie SK, Carvalho AA.
    J Med Genet; 1993 May; 30(5):385-7. PubMed ID: 8320700
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  • 2. Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families.
    Passos-Bueno MR, Moreira ES, Marie SK, Bashir R, Vasquez L, Love DR, Vainzof M, Iughetti P, Oliveira JR, Bakker E, Strachan T, Bushby K, Zatz M.
    J Med Genet; 1996 Feb; 33(2):97-102. PubMed ID: 8929943
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  • 3. A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy.
    Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SK, Pereira L, Akiyama J, Roberds SL, Campbell KP, Zatz M.
    Hum Mol Genet; 1995 Jul; 4(7):1163-7. PubMed ID: 8528203
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  • 6. Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate region.
    Passos-Bueno MR, Bashir R, Moreira ES, Vainzof M, Marie SK, Vasquez L, Iughetti P, Bakker E, Keers S, Stephenson A.
    Genomics; 1995 May 01; 27(1):192-5. PubMed ID: 7665169
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  • 7. Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus.
    Allamand V, Broux O, Bourg N, Richard I, Tischfield JA, Hodes ME, Conneally PM, Fardeau M, Jackson CE, Beckmann JS.
    Hum Mol Genet; 1995 Mar 01; 4(3):459-63. PubMed ID: 7795603
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  • 8. Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD.
    Passos-Bueno MR, Moreira ES, Vainzof M, Marie SK, Zatz M.
    Hum Mol Genet; 1996 Jun 01; 5(6):815-20. PubMed ID: 8776597
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  • 9. Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy families.
    Speer MC, Vance JM, Lennon-Graham F, Stajich JM, Viles KD, Gilchrist JM, Nigro V, McMichael R, Chutkow JG, Bartoloni L, Horrigan SK, Westbrook CA, Pericak-Vance MA.
    Hum Hered; 1998 Jun 01; 48(4):179-84. PubMed ID: 9694248
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  • 11. Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q.
    Speer MC, Yamaoka LH, Gilchrist JH, Gaskell CP, Stajich JM, Vance JM, Kazantsev A, Lastra AA, Haynes CS, Beckmann JS.
    Am J Hum Genet; 1992 Jun 01; 50(6):1211-7. PubMed ID: 1598902
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  • 12. The 10 autosomal recessive limb-girdle muscular dystrophies.
    Zatz M, de Paula F, Starling A, Vainzof M.
    Neuromuscul Disord; 2003 Sep 01; 13(7-8):532-44. PubMed ID: 12921790
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  • 16. A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage.
    Beckmann JS, Richard I, Hillaire D, Broux O, Antignac C, Bois E, Cann H, Cottingham RW, Feingold N, Feingold J.
    C R Acad Sci III; 1991 Sep 01; 312(4):141-8. PubMed ID: 1901754
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  • 17. Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence.
    Passos-Bueno MR, Terwilliger J, Ott J, Vainzof M, Love DR, Davies KE, Zatz M.
    Am J Med Genet; 1991 Jan 01; 38(1):140-6. PubMed ID: 2012126
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  • 18. Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G.
    Passos-Bueno MR, Vainzof M, Moreira ES, Zatz M.
    Am J Med Genet; 1999 Feb 19; 82(5):392-8. PubMed ID: 10069710
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