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Acta Paediatrica (Oslo, Norway : 1992)|March 30, 2004
Homozygous hypercholesterolaemia and ezetimibe: a case reportC J Hendriksz, G Norbury, S Tabrah, et al.Clinical Genetics|June 2, 2007
Multiplex ARMS analysis to detect 13 common mutations in familial hypercholesterolaemiaA Taylor, S Tabrah, D Wang, et al.Clinical Genetics|June 23, 2009
Multiplex ligation-dependent probe amplification analysis to screen for deletions and duplications of the LDLR gene in patients with familial hypercholesterolaemiaA Taylor, B Martin, D Wang, et al.Acta Paediatrica (Oslo, Norway : 1992)|June 11, 2004
Feeding infants with undiluted goat's milk can mimic tyrosinaemia type 1C J Hendriksz, J H WalterAtherosclerosis|August 1, 1988
DNA polymorphisms of the apolipoprotein genes--their use in the investigation of the genetic component of hyperlipidaemia and atherosclerosisS E HumphriesJournal of Inherited Metabolic Disease|September 10, 2005
Successful pregnancy in a treated patient with biotinidase deficiencyC J Hendriksz, M A Preece, A ChakrapaniTrends in Cardiovascular Medicine|January 20, 2011
The genetic contribution to the risk of thrombosis and cardiovascular diseaseS E HumphriesPrenatal Diagnosis|October 22, 2009
Noninvasive prenatal diagnosis of early onset primary dystonia I in maternal plasmaCathy Meaney, G NorburyJournal of Inherited Metabolic Disease|January 27, 2005
Pregnancy in a patient with mucopolysaccharidosis type IH homozygous for the W402X mutationC J Hendriksz, G M Moss, J E WraithPageof 808