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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.Heart & Lung : the Journal of Critical Care|May 1, 1994
Implantable cardioverter defibrillators: a guide for cliniciansT Davidson, S VanRiper, P Harper, 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.Journal of Clinical Pathology|July 30, 2008
Platelet function testing: practice among UK National External Quality Assessment Scheme for Blood Coagulation participants, 2006I Jennings, T A L Woods, S Kitchen, et al.Journal of Neurochemistry|February 1, 1996
Phosphorylation and activation of tryptophan hydroxylase by exogenous protein kinase AP A Johansen, I Jennings, R G Cotton, et al.Journal of Thrombosis and Haemostasis : JTH|December 17, 2003
Problems relating to the laboratory diagnosis of factor XIII deficiency: a UK NEQAS studyI Jennings, S Kitchen, T A L Woods, et al.Pageof 35