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[Surgical treatment of endocrine ophthalmopathy].
Rødahl E, Seland J, Olofsson J, Aanderud S, Kråkenes J. Rødahl E, et al. Tidsskr Nor Laegeforen. 1999 May 10;119(12):1737-42. Tidsskr Nor Laegeforen. 1999. PMID: 10380588 Norwegian.
Clinical manifestation of a novel PAX6 mutation Arg128Pro.
Bredrup C, Knappskog PM, Rødahl E, Boman H. Bredrup C, et al. Among authors: rodahl e. Arch Ophthalmol. 2008 Mar;126(3):428-30. doi: 10.1001/archopht.126.3.428. Arch Ophthalmol. 2008. PMID: 18332330 No abstract available.
Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19.
Bredrup C, Saunier S, Oud MM, Fiskerstrand T, Hoischen A, Brackman D, Leh SM, Midtbø M, Filhol E, Bole-Feysot C, Nitschké P, Gilissen C, Haugen OH, Sanders JS, Stolte-Dijkstra I, Mans DA, Steenbergen EJ, Hamel BC, Matignon M, Pfundt R, Jeanpierre C, Boman H, Rødahl E, Veltman JA, Knappskog PM, Knoers NV, Roepman R, Arts HH. Bredrup C, et al. Among authors: rodahl e. Am J Hum Genet. 2011 Nov 11;89(5):634-43. doi: 10.1016/j.ajhg.2011.10.001. Epub 2011 Oct 20. Am J Hum Genet. 2011. PMID: 22019273 Free PMC article.
83 results