Publications
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Filters: Author is MacDonald, Ian M [Clear All Filters]
Autosomal dominant macular dystrophy in a large Canadian family. Can J Ophthalmol. 2003;38(1):33-40.
A novel syndrome of congenital lid and punctal anomalies, corneal and chorioretinal dystrophy. Ophthalmic Genet. 2003;24(2):111-6.
Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation. Ophthalmology. 2002;109(10):1862-70.
