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JAMA Ophthalmology|July 9, 2016
Characterization of CDH3-Related Congenital Hypotrichosis With Juvenile Macular DystrophySarah Hull, Gavin Arno, Anthony G Robson, et al.Genome Announcements|August 15, 2015
High-Quality Draft Genome Sequence of Francisella tularensis subsp. holarctica Strain OR96-0246L M Atkins, M E Holder, N J Ajami, et al.Genome Announcements|March 26, 2016
Complete Genome Sequence of Turicibacter sp. Strain H121, Isolated from the Feces of a Contaminated Germ-Free MouseT A Auchtung, M E Holder, J R Gesell, et al.The British Journal of Ophthalmology|October 20, 2010
Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1Robert H Henderson, Donna S Mackay, Zheng Li, et al.Investigative Ophthalmology & Visual Science|August 29, 2007
Pseudoxanthoma elasticum with generalized retinal dysfunction, a common finding?Isabelle Audo, Olivier M Vanakker, Alaric Smith, et al.Ophthalmology|April 4, 2017
Benign Yellow Dot Maculopathy: A New Macular PhenotypeArundhati Dev Borman, Aleksandra Rachitskaya, Martina Suzani, et al.Acta Ophthalmologica|January 1, 2019
Unilateral pigmentary retinopathy: a retrospective case seriesMarie-Hélène Errera, Anthony G Robson, Tracey Wong, et al.Journal of Medical Genetics|July 10, 2008
ADVIRC is caused by distinct mutations in BEST1 that alter pre-mRNA splicingR Burgess, R E MacLaren, A E Davidson, et al.Human Mutation|January 3, 2013
RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophyAlice E Davidson, Panagiotis I Sergouniotis, Donna S Mackay, et al.The British Journal of Ophthalmology|May 29, 2024
Retinotopic cortical mapping in objective functional monitoring of macular therapyMarkus Ritter, Allan Hummer, Maximilian Pawloff, et al.Pageof 36