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Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1979
Mucolipidosis IV. Histopathology of conjunctiva, cornea, and skinK R Kenyon, I H Maumenee, W R Green, et al.Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 1, 1994
Ocular findings in trigonocephalyD Denis, L Genitori, J Bardot, et al.Ophthalmic Genetics|March 1, 1994
Visual outcome after surgery for Peters' anomalyS R Gollamudi, E I Traboulsi, W Chamon, et al.American Journal of Medical Genetics|October 1, 1984
Linkage analysis in lattice corneal dystrophyJ D Kivlin, E W Lovrien, I H Maumenee, et al.American Journal of Ophthalmology|January 23, 1998
Clinical features of autosomal dominant congenital nystagmus linked to chromosome 6p12J B Kerrison, R K Koenekoop, V J Arnould, et al.American Journal of Ophthalmology|October 1, 1980
Hereditary Fuchs' DystrophyP Rosenblum, W J Stark, I H Maumenee, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|March 1, 1983
Hereditary posterior microphthalmos with papillomacular fold and high hyperopiaM Spitznas, E Gerke, J B BatemanArchives of Dermatology|May 1, 1977
A cutaneous marker in the Hunter syndrome a report of four casesS D Prystowsky, I H Maumenee, R G Freeman, et al.American Journal of Ophthalmology|November 1, 1979
An analysis of visual acuity, visual fields, and disk cupping in childhood glaucomaA L Robin, H A Quigley, I P Pollack, et al.Investigative Ophthalmology & Visual Science|July 13, 2000
A CRX null mutation is associated with both Leber congenital amaurosis and a normal ocular phenotypeE Silva, J M Yang, Y Li, et al.Pageof 17