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Ophthalmic Genetics|January 14, 2016
3D Orbital Reconstruction in a Patient with Microphthalmos and a Large Orbital Cyst-A Case ReportD L Mourits, J Wolff, T Forouzanfar, et al.Ophthalmic Genetics|January 16, 2016
The TNF-α-308G/A Polymorphism is Not Associated with Ocular Chlamydia trachomatis Infection in Han Chinese ChildrenWenwen Xue, Qingzhong Wang, Zhiqiang Li, et al.Ophthalmic Genetics|January 16, 2016
A Patient with Keratoconus, Nanophthalmos, Lipodermoids, and Pigmentary RetinopathyFady K Sammouh, Tania A Baban, Elias L WarrakOphthalmic Genetics|January 16, 2016
SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association StudyMami Nishisako, Akira Meguro, Eiichi Nomura, et al.Ophthalmic Genetics|February 9, 2016
C8orf37 is mutated in Bardet-Biedl syndrome and constitutes a locus allelic to non-syndromic retinal dystrophiesArif O Khan, Eva Decker, Nadine Bachmann, et al.Ophthalmic Genetics|February 9, 2016
Choroideremia research: Report and perspectives on the second international scientific symposium for choroideremiaStephanie C Chan, Tania Bubela, Ioannis S Dimopoulos, et al.Ophthalmic Genetics|February 12, 2016
A novel homozygous MYO7A mutation involved in a Venezuelan population with high frequency of USHER1BHorbelys O Guzmán, Aura M Palacios, María I De Almada, et al.Ophthalmic Genetics|March 3, 2016
Further evidence for heredity of pterygiumVito Romano, Bernhard Steger, Adriana Kovacova, et al.Ophthalmic Genetics|February 26, 2016
Association study of the common polymorphisms in the folate-methionine pathway with retinoblastomaElaheh Soleimani, Kioomars Saliminejad, Mohammad Taghi Akbari, et al.Ophthalmic Genetics|September 3, 2015
Characterization of a Case of Pigmentary Retinopathy in Sanfilippo Syndrome Type IIIA Associated with Compound Heterozygous Mutations in the SGSH GeneJustin Wilkin, Natalie C Kerr, Kathryn W Byrd, et al.Pageof 185