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Archives of Ophthalmology (Chicago, Ill. : 1960)|October 26, 1999
Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 familiesS M Downes, F W Fitzke, G E Holder, et al.
Human Mutation|August 13, 2011
Digenic inheritance of mutations in FOXC1 and PITX2 : correlating transcription factor function and Axenfeld-Rieger disease severityDaniel Kelberman, Lily Islam, Susan E Holder, et al.
Archives of Family Medicine|April 1, 1993
Diagnostic and treatment guidelines on elder abuse and neglectS C Aravanis, R D Adelman, R Breckman, et al.
Investigative Ophthalmology & Visual Science|March 14, 2015
Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation of RBP3 Is Associated With High Myopia and Retinal DystrophyGavin Arno, Sarah Hull, Anthony G Robson, et al.
Ophthalmology|June 15, 2005
X-linked cone dysfunction syndrome with myopia and protanopiaMichel Michaelides, Samantha Johnson, Keith Bradshaw, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 7, 2001
Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1S M Downes, G E Holder, F W Fitzke, et al.
The Journal of Biological Chemistry|September 1, 1995
Identification, tissue-specific expression, and subcellular localization of the 80- and 71-kDa forms of myotonic dystrophy kinase proteinM Maeda, C S Taft, E W Bush, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|November 14, 2025
Unilateral pigmentary retinopathy in an Asian populationGeorge N Thomas, Sze Chuan Ong, Hwei Wuen Chan, et al.
Comparative Biochemistry and Physiology. Part A, Molecular & Integrative Physiology|February 15, 2022
Impairment of branchial and coronary blood flow reduces reproductive fitness, but not cardiac performance in paternal smallmouth bass (Micropterus dolomieu)Andreas Ekström, Tanya S Prystay, Alice E I Abrams, et al.
The British Journal of Ophthalmology|November 12, 2003
Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the alpha-subunit of cone specific transducin (GNAT2)M Michaelides, I A Aligianis, G E Holder, et al.
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