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Faucher M 1

Showing records 1 to 1 | Display all abstracts from Faucher M

13055 A common disease haplotype for the Q368STOP mutation of the myocilin gene in Australian and Canadian glaucoma families
Baird PN; Richardson AJ; Mackey DA; Craig JE; Faucher M; Raymond V
American Journal of Ophthalmology 2005; 140: 760-762

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