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M. Loyer
M. Loyer
McGill University
Biology
Genetics
Anatomy
Frameshift mutation
Diabetes mellitus
6
Papers
98
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In vivo Functional Analyses of Retinal Function by Multifocal Electroretinography in Unrelated Carriers of XRRP with the Same 2 Basepair Deletion in ORF15 of RPGR (2281_2282 del GG)
2003
Investigative Ophthalmology & Visual Science
G. Li
M. Loyer
Irma Lopez
H. Chakor
Collette K. Hand
R.C. Polomeno
J. Racine
Pierre Lachapelle
Guy A. Rouleau
Robert K. Koenekoop
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Molecular Studies of French Canadian Retinitis Pigmentosa Patients: Linkage analyses and Genotype-Phenotype Studies of a Genetic Isolate
2002
Investigative Ophthalmology & Visual Science
Robert K. Koenekoop
M. Loyer
Collette K. Hand
H Al Mahdi
M Papaioannou
O Dembinska
J. Racine
S Bhattacharya
Guy A. Rouleau
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Evaluation of the gene encoding the α subunit of cone transducin in Leber's congenital amaurosis and other retinal dystrophies
1996
Investigative Ophthalmology & Visual Science
M. Loyer
L. Wise
Elias I. Traboulsi
Irene H. Maumenee
Robert K. Koenekoop
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