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Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|October 1, 1987
Gene mapping of X-linked choroideremia with restriction fragment-length polymorphismsI M MacDonald, R M Sandre, A G Hunter, et al.The Medical Journal of Australia|April 17, 1976
Studies with prazosin--a new effective hypotensive agent. I. Open clinical study of prazosin in combination with other antihypertensive agentsA S Hua, I M Macdonald, J B Myers, et al.American Journal of Medical Genetics|August 1, 1989
Growth and development in thanatophoric dysplasiaI M MacDonald, A G Hunter, P M MacLeod, et al.Human Molecular Genetics|October 1, 1996
Expression of the dystrophin isoform Dp71 in differentiating human fetal myogenic culturesC N Tennyson, G Y Dally, P N Ray, et al.Molecular and Cellular Biology|May 1, 1986
Molecular cloning of cDNA for rat argininosuccinate lyase and its expression in rat hepatoma cell linesM A Lambert, L R Simard, P N Ray, et al.Neurology|September 25, 1998
Congenital cytoplasmic body myopathy with survival motor neuron gene deletion or Werdnig-Hoffmann diseaseJ Vajsar, T Balslev, P N Ray, et al.Clinical Genetics|December 9, 2009
Direct-to-consumer genetic testing: good, bad or benign?T Caulfield, N M Ries, P N Ray, et al.Journal of Medical Genetics|December 1, 1986
Molecular deletion analysis in Duchenne muscular dystrophyN S Thomas, P N Ray, R G Worton, et al.Journal of Medical Genetics|August 1, 1997
Monozygotic twins discordant for Aicardi syndromeT Costa, W Greer, G Rysiecki, et al.Journal of Intellectual Disability Research : JIDR|December 7, 2011
Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndromeG Costain, E W C Chow, P N Ray, et al.Pageof 14