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Journal Abstract Search

328 related items for PubMed ID: 8617508

  • 21. 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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  • 23. Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.
    Ben Othmane K, Ben Hamida M, Pericak-Vance MA, Ben Hamida C, Blel S, Carter SC, Bowcock AM, Petruhkin K, Gilliam TC, Roses AD.
    Nat Genet; 1992 Dec; 2(4):315-7. PubMed ID: 1303286
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  • 27. Physical and genetic mapping of the macular corneal dystrophy locus on chromosome 16q and exclusion of TAT and LCAT as candidate genes.
    Liu NP, Dew-Knight S, Jonasson F, Gilbert JR, Klintworth GK, Vance JM.
    Mol Vis; 2000 Jun 19; 6():95-100. PubMed ID: 10869098
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  • 35. The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12.
    Moreira ES, Vainzof M, Marie SK, Sertié AL, Zatz M, Passos-Bueno MR.
    Am J Hum Genet; 1997 Jul 19; 61(1):151-9. PubMed ID: 9245996
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  • 37. Homozygosity and linkage disequilibrium mapping of autosomal recessive distal myopathy (Nonaka distal myopathy).
    Asaka T, Ikeuchi K, Okino S, Takizawa Y, Satake R, Nitta E, Komai K, Endo K, Higuchi S, Oyake T, Yoshimura T, Suenaga A, Uyama E, Saito T, Konagaya M, Sunohara N, Namba R, Takada H, Honke K, Nishina M, Tanaka H, Shinagawa M, Tanaka K, Matsushima A, Tsuji S, Takamori M.
    J Hum Genet; 2001 Jul 19; 46(11):649-55. PubMed ID: 11721884
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  • 40. A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.
    Guilford P, Ben Arab S, Blanchard S, Levilliers J, Weissenbach J, Belkahia A, Petit C.
    Nat Genet; 1994 Jan 19; 6(1):24-8. PubMed ID: 8136828
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