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British Journal of Haematology|October 16, 1999
A novel mutation of delta-aminolaevulinate dehydratase in a healthy child with 12% erythrocyte enzyme activityR Akagi, Y Yasui, P Harper, et al.Journal of Oral and Maxillofacial Surgery : Official Journal of the American Association of Oral and Maxillofacial Surgeons|March 1, 1997
Muscle activity during mandibular movements in normal and mandibular retrognathic subjectsR P Harper, H de Bruin, I BurceaAmerican Journal of Medical Genetics|July 26, 1996
Characterization of six mutations in exon 37 of neurofibromatosis type 1 geneM Upadhyaya, M Osborn, J Maynard, et al.Journal of Internal Medicine|April 24, 2010
Erythropoietic protoporphyria in Sweden: demographic, clinical, biochemical and genetic characteristicsS Wahlin, Y Floderus, P Stål, et al.Australian Veterinary Journal|January 1, 1990
Congenital biliary atresia and jaundice in lambs and calvesP Harper, J W Plant, D B UngerLancet (London, England)|March 4, 1989
Distinction of Becker from limb-girdle muscular dystrophy by means of dystrophin cDNA probesA Norman, N Thomas, J Coakley, et al.Scandinavian Journal of Clinical and Laboratory Investigation|May 15, 2002
Non-viral mediated gene transfer of porphobilinogen deaminase into mammalian cellsA Johansson, C Möller, P Gellerfors, et al.American Journal of Orthodontics and Dentofacial Orthopedics : Official Publication of the American Association of Orthodontists, Its Constituent Societies, and the American Board of Orthodontics|January 1, 1987
Lateral pterygoid muscle activity in mandibular retrognathism and response to mandibular advancement surgeryR P Harper, H de Bruin, I BurceaOptics Express|May 3, 2014
Unrepeatered DPSK transmission over 360 km SMF-28 fibre using URFL based amplificationP Rosa, J-D Ania-Castañón, P HarperClinical Genetics|October 10, 2002
Acute intermittent porphyria in Sweden. Molecular, functional and clinical consequences of some new mutations found in the porphobilinogen deaminase geneY Floderus, P M Shoolingin-Jordan, P HarperPageof 63