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328 related items for PubMed ID: 8617508

  • 1. 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]

  • 2. 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]

  • 3. [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
    [Abstract] [Full Text] [Related]

  • 4. YAC contigs of the Rab1 and wobbler (wr) spinal muscular atrophy gene region on proximal mouse chromosome 11 and of the homologous region on human chromosome 2p.
    Wedemeyer N, Lengeling A, Ronsiek M, Korthaus D, Baer K, Wuttke M, Jockusch H.
    Genomics; 1996 Mar 15; 32(3):447-54. PubMed ID: 8838809
    [Abstract] [Full Text] [Related]

  • 5. [Miyoshi distal muscular dystrophy].
    Hirabayashi K.
    Nihon Rinsho; 1997 Dec 15; 55(12):3190-4. PubMed ID: 9436434
    [Abstract] [Full Text] [Related]

  • 6. A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey.
    Dinçer P, Leturcq F, Richard I, Piccolo F, Yalnizoglu D, de Toma C, Akçören Z, Broux O, Deburgrave N, Brenguier L, Roudaut C, Urtizberea JA, Jung D, Tan E, Jeanpierre M, Campbell KP, Kaplan JC, Beckmann JS, Topaloglu H.
    Ann Neurol; 1997 Aug 15; 42(2):222-9. PubMed ID: 9266733
    [Abstract] [Full Text] [Related]

  • 7. Generation of a 3-Mb PAC contig spanning the Miyoshi myopathy/limb-girdle muscular dystrophy (MM/LGMD2B) locus on chromosome 2p13.
    Liu J, Wu C, Bossie K, Bejaoui K, Hosler BA, Gingrich JC, Ben Hamida M, Hentati F, Schurr E, de Jong PJ, Brown RH.
    Genomics; 1998 Apr 01; 49(1):23-9. PubMed ID: 9570945
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21.
    Starling A, Kok F, Passos-Bueno MR, Vainzof M, Zatz M.
    Eur J Hum Genet; 2004 Dec 01; 12(12):1033-40. PubMed ID: 15367920
    [Abstract] [Full Text] [Related]

  • 11. 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 01; 119 ( Pt 6)():1895-909. PubMed ID: 9009996
    [Abstract] [Full Text] [Related]

  • 12. Integrated radiation hybrid map of human chromosome 2p13: possible involvement of dynactin in neuromuscular diseases.
    Korthaus D, Wedemeyer N, Lengeling A, Ronsiek M, Jockusch H, Schmitt-John T.
    Genomics; 1997 Jul 15; 43(2):242-4. PubMed ID: 9244444
    [Abstract] [Full Text] [Related]

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  • 14. YAC and cosmid contigs encompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9q31.
    Miyake M, Nakahori Y, Matsushita I, Kobayashi K, Mizuno K, Hirai M, Kanazawa I, Nakagome Y, Tokunaga K, Toda T.
    Genomics; 1997 Mar 01; 40(2):284-93. PubMed ID: 9119396
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  • 18. 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 Mar 01; 312(4):141-8. PubMed ID: 1901754
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  • 20. [Calpain-3 gene defect causing limb gird muscular dystrophy in a Hungarian family].
    Horváth R, Walter MC, Lochmüller H, Hübner A, Karcagi V, Pikó H, Timár L, Komoly S.
    Ideggyogy Sz; 2005 Jan 20; 58(1-2):52-8. PubMed ID: 15884399
    [Abstract] [Full Text] [Related]

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