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Optics Express
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June 18, 2009
Forward scattering measurement device with a high angular resolution
David 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 2
Hana 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 imperfecta
Bozena 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 family
Pascal Escher, Peter Gouras, Raphaël Roduit, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 4) with videos related to
Sort By:
Page
of 1
Optics Express
|
June 18, 2009
Forward scattering measurement device with a high angular resolution
David 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 2
Hana 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 imperfecta
Bozena 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 family
Pascal Escher, Peter Gouras, Raphaël Roduit, et al.
Page
of 1