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Investigative Ophthalmology & Visual Science|January 14, 2000
Genetic heterogeneity of the Coppock-like cataract: a mutation in CRYBB2 on chromosome 22q11.2D Gill, R Klose, F L Munier, et al.
Ophthalmic Genetics|November 12, 1998
Rhodopsin C110Y mutation causes a type 2 autosomal dominant retinitis pigmentosaE Millá, E Héon, P A Grounauer, et al.
Neuro-Chirurgie|March 23, 2010
[Orbitotemporal facial involvement in type 1 neurofibromatosis (NF1)]B Rilliet, B Pittet, D Montandon, et al.
Anesthesiology|December 1, 1992
Intelligent alarms reduce anesthesiologist's response time to critical faultsD R Westenskow, J A Orr, F H Simon, et al.
The British Journal of Ophthalmology|May 5, 2006
Primary lymphoma of the lacrimal sac: an EORTC ophthalmic oncology task force studyL D Sjö, E Ralfkiaer, B R Juhl, et al.
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