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E Héon

Showing results (1-10 of 54) with videos related to

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The British Journal of Ophthalmology|April 26, 2003
Predictive DNA testing in ophthalmology: view 1E Héon
Eye (London, England)|June 30, 2012
Outer retinal structural anomaly due to frameshift mutation in CACNA1F geneA Vincent, E Héon
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 6, 1998
Helicoid peripapillary chorioretinal degeneration in abetalipoproteinemiaA M Wong, E Héon
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|June 1, 1997
The genetics of glaucoma: an updateS Liu, J C Cheung, E Héon
Clinical Genetics|June 14, 2000
Recent advances in the molecular basis of inherited photoreceptor degenerationG Clarke, E Héon, R R McInnes
Clinical Genetics|May 20, 2015
Exploration of the cognitive, adaptive and behavioral functioning of patients affected with Bardet-Biedl syndromeE N Kerr, A Bhan, E Héon
Clinical Genetics|December 9, 2009
Ciliary dysfunction and obesityC A Mok, E Héon, M Zhen
American Journal of Ophthalmology|April 1, 1995
Retinoma associated with vitreous seedingG T Lueder, E Héon, B L Gallie
The British Journal of Ophthalmology|April 26, 2003
Predictive DNA testing in ophthalmologyD A Mackey, E Héon, A R Webster
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.
Pageof 6

Showing results (1-10 of 54) with videos related to

Sort By:
Pageof 6
The British Journal of Ophthalmology|April 26, 2003
Predictive DNA testing in ophthalmology: view 1E Héon
Eye (London, England)|June 30, 2012
Outer retinal structural anomaly due to frameshift mutation in CACNA1F geneA Vincent, E Héon
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 6, 1998
Helicoid peripapillary chorioretinal degeneration in abetalipoproteinemiaA M Wong, E Héon
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|June 1, 1997
The genetics of glaucoma: an updateS Liu, J C Cheung, E Héon
Clinical Genetics|June 14, 2000
Recent advances in the molecular basis of inherited photoreceptor degenerationG Clarke, E Héon, R R McInnes
Clinical Genetics|May 20, 2015
Exploration of the cognitive, adaptive and behavioral functioning of patients affected with Bardet-Biedl syndromeE N Kerr, A Bhan, E Héon
Clinical Genetics|December 9, 2009
Ciliary dysfunction and obesityC A Mok, E Héon, M Zhen
American Journal of Ophthalmology|April 1, 1995
Retinoma associated with vitreous seedingG T Lueder, E Héon, B L Gallie
The British Journal of Ophthalmology|April 26, 2003
Predictive DNA testing in ophthalmologyD A Mackey, E Héon, A R Webster
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.
Pageof 6