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Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1995
Immunohistochemical localization of fibrillin in human ocular tissues. Relevance to the Marfan syndromeH M Wheatley, E I Traboulsi, B E Flowers, et al.American Journal of Ophthalmology|February 15, 1986
Genetic linkage analysis of autosomal dominant congenital cataractsJ B Bateman, M A Spence, M L Marazita, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|October 1, 1985
Classification of congenital and early onset retinitis pigmentosaS G Foxman, J R Heckenlively, J B Bateman, et al.Ophthalmology|October 1, 1981
Cycloplegic refraction in esotropic children. Cyclopentolate versus atropineA L Rosenbaum, J B Bateman, D L Bremer, et al.Journal of Pediatric Ophthalmology and Strabismus|May 1, 1986
Ligneous conjunctivitis: an autosomal recessive disorderJ B Bateman, T H Pettit, S J Isenberg, et al.Journal of Pediatric Ophthalmology and Strabismus|July 1, 1987
The Rieger syndrome and a chromosome 13 deletionR A Stathacopoulos, J B Bateman, R S Sparkes, et al.The Western Journal of Medicine|October 1, 1991
Molecular genetics of retinitis pigmentosaD B Farber, J R Heckenlively, R S Sparkes, et al.Ophthalmology|June 17, 1998
Menkes disease. New ocular and electroretinographic findingsR C Ferreira, J R Heckenlively, J H Menkes, et al.Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 1, 1985
Eye movement abnormalities in rod monochromatism and blue-cone monochromatismR D Yee, M K Farley, J B Bateman, et al.American Journal of Medical Genetics|July 16, 1999
Ocular anterior chamber dysgenesis in craniosynostosis syndromes with a fibroblast growth factor receptor 2 mutationK Okajima, L K Robinson, M A Hart, et al.Pageof 17