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Nature Genetics|July 11, 2000
Genetic basis of total colourblindness among the Pingelapese islandersO H Sundin, J M Yang, Y Li, et al.
Human Genetics|November 1, 1990
Assignment of the Nance-Horan syndrome to the distal short arm of the X chromosomeD Zhu, D M Alcorn, S E Antonarakis, et al.
American Journal of Ophthalmology|September 27, 2000
Acute megakaryoblastic leukemia in Down syndrome: orbital infiltrationJ L Olson, M J May, L Stork, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 1, 1990
Congenital hypertrophy of the retinal pigment epithelium predicts colorectal polyposis in Gardner's syndromeE I Traboulsi, I H Maumenee, A J Krush, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 16, 1999
Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3J B Kerrison, V J Arnould, J M Ferraz Sallum, et al.
Science (New York, N.Y.)|August 25, 1989
Molecular genetics of human blue cone monochromacyJ Nathans, C M Davenport, I H Maumenee, et al.
American Journal of Human Genetics|November 1, 1993
Genetic heterogeneity among blue-cone monochromatsJ Nathans, I H Maumenee, E Zrenner, et al.
Clinical Genetics|July 1, 1988
Recombinational event between Norrie disease and DXS7 lociJ T Ngo, M A Spence, V Cortessis, et al.
Survey of Ophthalmology|November 30, 2000
Ocular colobomataB C Onwochei, J W Simon, J B Bateman, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 1, 1993
The effectiveness of daily wear contact lenses for the correction of infantile aphakiaD Neumann, B A Weissman, S J Isenberg, et al.
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