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Ophthalmic Genetics|February 21, 2013
Clinical phenotype in ten unrelated Japanese patients with mutations in the EYS geneKimiko Suto, Katsuhiro Hosono, Masayo Takahashi, et al.Ophthalmic Genetics|September 5, 2013
A novel CYP1B1 mutation with congenital glaucoma and total aniridiaSultan Alzuhairy, Khaled K Abu-Amero, Sami Al-Shahwan, et al.Ophthalmic Genetics|May 4, 2013
Genetic variation of superoxide dismutases in patients with primary open-angle glaucomaDragana Celojevic, Staffan Nilsson, Lada Kalaboukhova, et al.Ophthalmic Genetics|May 8, 2013
Optic disc dysplasia in poland syndromeSteven D Maxfield, Mitchell B StromingerOphthalmic Genetics|August 1, 2014
Enucleation Refusal for Retinoblastoma: A Global StudyCristina Olteanu, Helen DimarasOphthalmic Genetics|March 26, 2013
Falciform macular folds and chromosome 22q11.2: evidence in support of a locus for familial exudative vitreoretinopathy (FEVR)Jarel K Gandhi, Travis T Tollefson, David G TelanderOphthalmic Genetics|January 8, 2013
Common single nucleotide polymorphisms and keratoconus in the Han Chinese populationYani Wang, Tianbo Jin, Xuehui Zhang, et al.Ophthalmic Genetics|May 4, 2012
Reduced L- and M- and increased S-cone functions in an infant with thyroid hormone resistance due to mutations in the THRβ2 geneAvery H Weiss, John P Kelly, Darren Bisset, et al.Ophthalmic Genetics|December 11, 2012
Congenital accessory palpebral aperture--an addition to the spectrum of Delleman syndromeAditi Manudhane, Ritu Arora, Seema Kapoor, et al.Ophthalmic Genetics|January 1, 2013
Copy number variant analysis in CHM to detect duplications underlying choroideremiaJonathan Y Chi, Ian M MacDonald, Stacey HumePageof 185