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Eye (London, England)|November 13, 2010
BEST1-related autosomal dominant vitreoretinochoroidopathy: a degenerative disease with a range of developmental ocular anomaliesA Vincent, C McAlister, C Vandenhoven, et al.Eye (London, England)|December 9, 2017
Specific retinal phenotype in early IQCB1-related diseaseA Vincent, A AlAli, H MacDonald, et al.Clinical Genetics|June 21, 2018
IFT80 mutations cause a novel complex ciliopathy phenotype with retinal degenerationJ Moran, K G Sanderson, J Maynes, et al.Clinical Genetics|June 14, 2000
Recent advances in the molecular basis of inherited photoreceptor degenerationG Clarke, E Héon, R R McInnesClinical Genetics|May 20, 2015
Exploration of the cognitive, adaptive and behavioral functioning of patients affected with Bardet-Biedl syndromeE N Kerr, A Bhan, E HéonAmerican Journal of Ophthalmology|April 1, 1995
Retinoma associated with vitreous seedingG T Lueder, E Héon, B L GallieClinical Genetics|October 16, 2016
The combination of vestibular impairment and congenital sensorineural hearing loss predisposes patients to ocular anomalies, including Usher syndromeS Kletke, V Batmanabane, T Dai, et al.Developments in Ophthalmology|July 25, 2003
A molecular perspective on corneal dystrophiesA L Vincent, D Rootman, F L Munier, et al.Eye (London, England)|September 16, 2008
Retinal microstructure in patients with EFEMP1 retinal dystrophy evaluated by Fourier domain OCTC Gerth, R J Zawadzki, J S Werner, et al.Pageof 125