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Human Mutation|January 1, 1997
Spectrum of LDL receptor gene mutations in heterozygous familial hypercholesterolemiaI N Day, R A Whittall, S D O'Dell, et al.Paediatric and Perinatal Epidemiology|August 8, 2001
Birthweight, vitamin D receptor genotype and the programming of osteoporosisE M Dennison, N K Arden, R W Keen, et al.Human Genetics|April 17, 1998
Analysis of low density lipoprotein receptor gene mutations and microsatellite haplotypes in Greek FH heterozygous children: six independent ancestors account for 60% of probandsJ Traeger-Synodinos, N Mavroidis, E Kanavakis, et al.Journal of Dairy Science|March 14, 2016
Virtual milk for modelling and simulation of dairy processesM T Munir, Y Zhang, W Yu, et al.International Journal of Pharmaceutics|October 12, 2010
Extrusion-spheronisation of highly loaded 5-ASA multiparticulate dosage formsG Di Pretoro, L Zema, A Gazzaniga, et al.The British Journal of Surgery|February 15, 2000
Mutations of the cationic trypsinogen gene in patients with hereditary pancreatitisJ E Creighton, R Lyall, D I Wilson, et al.European Cells & Materials|June 29, 2011
Developmental plasticity of human foetal femur-derived cells in pellet culture: self assembly of an osteoid shell around a cartilaginous coreA T El-Serafi, D I Wilson, H I Roach, et al.American Journal of Health-System Pharmacy : AJHP : Official Journal of the American Society of Health-System Pharmacists|April 18, 2000
Hospital pharmacy service provision in Australia--1998S G Wilson, M Tsui, N Tong, et al.Biofouling|February 15, 2012
Characterising the structure of photosynthetic biofilms using fluid dynamic gaugingB Salley, P W Gordon, A J McCormick, et al.Lancet (London, England)|September 5, 1992
Deletions within chromosome 22q11 in familial congenital heart diseaseD I Wilson, J A Goodship, J Burn, et al.Pageof 12