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Editorial Article

A tribute to Mette Warburg

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Pages 123-125 | Published online: 08 Jul 2009

References

  • Warburg M. If only you do it well: Autobiography. Ophthalmic Genet 1996; 17: 131–144
  • Piguet B, Heon E, Munier F L, Grounauer P A, Niemeyer G, Butler N, Schorderet D F, Sheffield V C, Stone E M. Full characterization of the maculopathy associated with an Arg-172-Trp mutation in the rds/peripherin gene. Ophthalmic Genet 1996; 17: 175–186
  • Traboulsi E I, Apostolides J, Giardiello F M, Krush A J, Booker S V, Hamilton S R, Maumenee I E. Pigmented ocular fundus lesions and apc mutations in familial adenomatous polyposis. Ophthalmic Genet 1996; 17: 167–174
  • Caballero M, Veske A, Rodriguez J J, Lugo N, Schroeder B, Hesse L, Gal A. Two novel mutations in the Norrie disease gene associated with the classical ocular phenotype. Ophthalmic Genet 1996; 17: 187–191
  • Haim M, Grundmann K, Gal A, Rosenberg T. Novel rhodopsin mutation (M216R) in a Danish family with autosomal dominant retinitis pigmentosa. Ophthalmic Genet 1996; 17: 193–197
  • Coote M A, McCartney P J, Wilkinson R, Mackey D A. The ‘gist’ score: ranking glaucoma for genetic studies. Ophthalmic Genet 1996; 17: 199–208
  • Sack J, Healey D L, De Graaf A P, Wilkinson R M, Wilkinson C H, Barbour J M, Coote M A, McCartney P J, Rain J L, Cooper R L, Ring M A, Mackey D A. The problem of overlapping glaucoma families in the Glaucoma Inheritance Study in Tasmania (gist). Ophthalmic Genet 1996; 17: 209–214
  • Nickells R W, Zack D J. Apoptosis in ocular disease: a molecular overview. Ophthalmic Genet 1996; 17: 145–165

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