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Journal Abstract Search

152 related items for PubMed ID: 12913210

  • 1. A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q32.1-32.2.
    Palenzuela L, Andreu AL, Gàmez J, Vilà MR, Kunimatsu T, Meseguer A, Cervera C, Fernandez Cadenas I, van der Ven PF, Nygaard TG, Bonilla E, Hirano M.
    Neurology; 2003 Aug 12; 61(3):404-6. PubMed ID: 12913210
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  • 3. Limb-girdle muscular dystrophy is closely linked to the fibrillin locus on chromosome 15.
    Velinov M, Sarfarazi M, Young K, Hodes ME, Conneally PM, Jackson CE, Tsipouras P.
    Connect Tissue Res; 1993 Aug 12; 29(1):13-21. PubMed ID: 8339542
    [Abstract] [Full Text] [Related]

  • 4. Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21.
    van der Kooi AJ, van Meegen M, Ledderhof TM, McNally EM, de Visser M, Bolhuis PA.
    Am J Hum Genet; 1997 Apr 12; 60(4):891-5. PubMed ID: 9106535
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  • 5. 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 Apr 12; 48(4):179-84. PubMed ID: 9694248
    [Abstract] [Full Text] [Related]

  • 6. 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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  • 7. Autosomal dominant limb-girdle muscular dystrophy: a large kindred with evidence for anticipation.
    Gamez J, Navarro C, Andreu AL, Fernandez JM, Palenzuela L, Tejeira S, Fernandez-Hojas R, Schwartz S, Karadimas C, DiMauro S, Hirano M, Cervera C.
    Neurology; 2001 Feb 27; 56(4):450-4. PubMed ID: 11222786
    [Abstract] [Full Text] [Related]

  • 8. 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 27; 50(6):1211-7. PubMed ID: 1598902
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  • 9. 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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  • 10. Development of a microsatellite genetic map spanning 5q31-q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9.
    Yamaoka LH, Westbrook CA, Speer MC, Gilchrist JM, Jabs EW, Schweins EG, Stajich JM, Gaskell PC, Roses AD, Pericak-Vance MA.
    Neuromuscul Disord; 1994 May 01; 4(5-6):471-5. PubMed ID: 7881291
    [Abstract] [Full Text] [Related]

  • 11. Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin.
    Moreira ES, Wiltshire TJ, Faulkner G, Nilforoushan A, Vainzof M, Suzuki OT, Valle G, Reeves R, Zatz M, Passos-Bueno MR, Jenne DE.
    Nat Genet; 2000 Feb 01; 24(2):163-6. PubMed ID: 10655062
    [Abstract] [Full Text] [Related]

  • 12. Refined genetic location of the chromosome 2p-linked progressive muscular dystrophy gene.
    Illarioshkin SN, Ivanova-Smolenskaya IA, Tanaka H, Poleshchuk VV, Markova ED, Tsuji S.
    Genomics; 1997 Jun 01; 42(2):345-8. PubMed ID: 9192858
    [Abstract] [Full Text] [Related]

  • 13. 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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  • 14. Candidate-gene testing for orphan limb-girdle muscular dystrophies.
    Aurino S, Piluso G, Saccone V, Cacciottolo M, D'Amico F, Dionisi M, Totaro A, Belsito A, Di Vicino U, Nigro V.
    Acta Myol; 2008 Dec 01; 27(3):90-7. PubMed ID: 19472918
    [Abstract] [Full Text] [Related]

  • 15. 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 Dec 01; 312(4):141-8. PubMed ID: 1901754
    [Abstract] [Full Text] [Related]

  • 16. 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 01; 30(5):385-7. PubMed ID: 8320700
    [Abstract] [Full Text] [Related]

  • 17. A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13-p12.
    Jarry J, Rioux MF, Bolduc V, Robitaille Y, Khoury V, Thiffault I, Tétreault M, Loisel L, Bouchard JP, Brais B.
    Brain; 2007 Feb 01; 130(Pt 2):368-80. PubMed ID: 17008331
    [Abstract] [Full Text] [Related]

  • 18. 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
    [Abstract] [Full Text] [Related]

  • 19. Heterogeneity in familial dominant Paget disease of bone and muscular dystrophy.
    Waggoner B, Kovach MJ, Winkelman M, Cai D, Khardori R, Gelber D, Kimonis VE.
    Am J Med Genet; 2002 Mar 15; 108(3):187-91. PubMed ID: 11891683
    [Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]

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