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Sylvain Bolay

Showing results (1-10 of 4) with videos related to

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Optics Express|June 18, 2009
Forward scattering measurement device with a high angular resolutionDavid Roßkamp, Frederic Truffer, Sylvain Bolay, et al.
Ophthalmology|November 14, 2008
A new locus for congenital cataract, microcornea, microphthalmia, and atypical iris coloboma maps to chromosome 2Hana Abouzeid, Françoise M Meire, Ihab Osman, et al.
American Journal of Human Genetics|February 10, 2009
Mutations in CNNM4 cause recessive cone-rod dystrophy with amelogenesis imperfectaBozena Polok, Pascal Escher, Aude Ambresin, et al.
Human Mutation|November 14, 2008
Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same familyPascal Escher, Peter Gouras, Raphaël Roduit, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Optics Express|June 18, 2009
Forward scattering measurement device with a high angular resolutionDavid Roßkamp, Frederic Truffer, Sylvain Bolay, et al.
Ophthalmology|November 14, 2008
A new locus for congenital cataract, microcornea, microphthalmia, and atypical iris coloboma maps to chromosome 2Hana Abouzeid, Françoise M Meire, Ihab Osman, et al.
American Journal of Human Genetics|February 10, 2009
Mutations in CNNM4 cause recessive cone-rod dystrophy with amelogenesis imperfectaBozena Polok, Pascal Escher, Aude Ambresin, et al.
Human Mutation|November 14, 2008
Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same familyPascal Escher, Peter Gouras, Raphaël Roduit, et al.
Pageof 1