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Investigative Ophthalmology & Visual Science|September 28, 2007
The Roles of PAX6 and SOX2 in Myopia: lessons from the 1958 British Birth CohortClaire L Simpson, Pirro Hysi, Shomi S Bhattacharya, et al.Human Molecular Genetics|January 9, 2013
ATR localizes to the photoreceptor connecting cilium and deficiency leads to severe photoreceptor degeneration in miceLourdes Valdés-Sánchez, Berta De la Cerda, Francisco J Diaz-Corrales, et al.Advanced Materials (Deerfield Beach, Fla.)|March 7, 2019
High-Entropy Oxides: Fundamental Aspects and Electrochemical PropertiesAbhishek Sarkar, Qingsong Wang, Alexander Schiele, et al.Nutrition (Burbank, Los Angeles County, Calif.)|April 1, 1997
Mononuclear blood cell magnesium content and serum magnesium concentration in critically ill hypomagnesemic patients after replacement therapyG S Sacks, R O Brown, R N Dickerson, et al.Investigative Ophthalmology & Visual Science|March 11, 2000
A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13A Hameed, S Khaliq, M Ismail, et al.Human Genetics|December 6, 2001
A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effectD L Thiselton, C Alexander, A Morris, et al.Molecular Vision|August 8, 2007
Study of p.N247S KERA mutation in a British family with cornea planaPetra Liskova, Pirro G Hysi, Denise Williams, et al.Human Genetics|January 1, 1992
Localisation of the gene for Norrie disease to between DXS7 and DXS426 on XpS Lindsay, D L Thiselton, J B Bateman, et al.Human Molecular Genetics|May 1, 1996
Gene transfer into the mouse retina mediated by an adeno-associated viral vectorR R Ali, M B Reichel, A J Thrasher, et al.Human Reproduction (Oxford, England)|July 12, 2013
Assisted reproductive technology in Europe, 2009: results generated from European registers by ESHREA P Ferraretti, V Goossens, M Kupka, et al.Pageof 144