Robberecht K - Search Results

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Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosa.

Coppieters F, Leroy BP, Beysen D, Hellemans J, De Bosscher K, Haegeman G, Robberecht K, Wuyts W, Coucke PJ, De Baere E. Coppieters F, et al. Among authors: robberecht k. Am J Hum Genet. 2007 Jul;81(1):147-57. doi: 10.1086/518426. Epub 2007 May 24. Am J Hum Genet. 2007. PMID: 17564971 Free PMC article.

Ptosis as an associated finding in maternally inherited diabetes and deafness.

Robberecht K, Decock C, Stevens A, Seneca S, De Bleecker J, Leroy BP. Robberecht K, et al. Ophthalmic Genet. 2010 Dec;31(4):240-3. doi: 10.3109/13816810.2010.520297. Ophthalmic Genet. 2010. PMID: 21067488

Eyelashes on an extruding porous polyethylene orbital implant.

Robberecht K, Berghmans L, Kestelyn P, Decock C. Robberecht K, et al. Int Ophthalmol. 2011 Feb;31(1):21-2. doi: 10.1007/s10792-010-9395-7. Epub 2010 Sep 21. Int Ophthalmol. 2011. PMID: 20857174

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