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Journal Abstract Search
63 related items for PubMed ID: 11594343
41. X-linked vacuolar myopathies: two separate loci and refined genetic mapping. Auranen M, Villanova M, Muntoni F, Fardeau M, Scherer SW, Kalino H, Minassian BA. Ann Neurol; 2000 May; 47(5):666-9. PubMed ID: 10805342 [Abstract] [Full Text] [Related]
42. X-linked recessive inheritance of radial ray deficiencies in a family with four affected males. Galjaard RJ, Kostakoglu N, Hoogeboom JJ, Breedveld GJ, van der Linde HC, Hovius SE, Oostra BA, Sandkuijl LA, Akarsu AN, Heutink P. Eur J Hum Genet; 2001 Sep; 9(9):653-8. PubMed ID: 11571552 [Abstract] [Full Text] [Related]
48. Evidence for genetic heterogeneity in families with congenital motor nystagmus (CN). Oetting WS, Armstrong CM, Holleschau AM, DeWan AT, Summers GC. Ophthalmic Genet; 2000 Dec 12; 21(4):227-33. PubMed ID: 11135493 [Abstract] [Full Text] [Related]