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Annals of Human Genetics|September 1, 1996
Identification of an E689K substitution as the molecular basis of the human acid alpha-glucosidase type 4 allozyme (GAA*4)M L Huie, M Menaker, P J McAlpine, et al.Transfusion|May 1, 1996
Assignment of the gene(s) governing Froese and Swann blood group polymorphism to chromosome 17qT Zelinski, I McKeown, P J McAlpine, et al.Journal of Medical Genetics|April 1, 1985
An autosomal dominant syndrome with 'acromegaloid' features and thickened oral mucosaH E Hughes, P J McAlpine, D W Cox, et al.Journal of Medical Genetics|December 1, 1977
A 'new' syndrome of mental retardation with characteristic facies and brachyphalangyA G Hunter, P J McAlpine, N L Rudd, et al.American Journal of Medical Genetics|June 1, 1982
Brief clinical report: ring chromosome 17 in a mentally retarded young man - clinical, cytogenetic, and biochemical investigationsA E Chudley, P D Pabello, P J McAlpine, et al.Human Genetics|October 1, 1993
Identification of an uncommon haptoglobin type using DNA and protein analysisS L Marles, P J McAlpine, T Zelinski, et al.Genomics|October 1, 1991
The cloned butyrylcholinesterase (BCHE) gene maps to a single chromosome site, 3q26P W Allderdice, H A Gardner, D Galutira, et al.American Journal of Medical Genetics|September 1, 1988
Developmental delay, short stature, and minor facial anomalies in a child with ring chromosome 16B N Chodirker, M Ray, P J McAlpine, et al.Genome|November 6, 2002
Genetic diversity among Canadienne, Brown Swiss, Holstein, and Jersey cattle of Canada based on 15 bovine microsatellite markersC Hansen, J N B Shrestha, R J Parker, et al.Pageof 429