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European Heart Journal|July 7, 2009
First locus for primary pulmonary vein stenosis maps to chromosome 2qIngrid van de Laar, Marja Wessels, Ingrid Frohn-Mulder, et al.European Journal of Human Genetics : EJHG|August 27, 2009
Genome-wide linkage analysis in a Dutch multigenerational family with attention deficit hyperactivity disorderRinus Vegt, Aida M Bertoli-Avella, Joke H M Tulen, et al.Neuroscience Letters|August 24, 1999
The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's diseaseB S Harhangi, M J Farrer, S Lincoln, et al.European Journal of Epidemiology|February 24, 2007
Heritabilities, apolipoprotein E, and effects of inbreeding on plasma lipids in a genetically isolated population: the Erasmus Rucphen Family StudyAaron Isaacs, Fakhredin A Sayed-Tabatabaei, Yurii S Aulchenko, et al.The Journal of Clinical Endocrinology and Metabolism|April 19, 2007
Epistatic effect of cholesteryl ester transfer protein and hepatic lipase on serum high-density lipoprotein cholesterol levelsAaron Isaacs, Yurii S Aulchenko, Albert Hofman, et al.European Journal of Epidemiology|June 30, 2010
Insulin-resistance and metabolic syndrome are related to executive function in women in a large family-based studyM Schuur, P Henneman, J C van Swieten, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 16, 2007
Polymorphisms of the renin-angiotensin system are associated with blood pressure, atherosclerosis and cerebral white matter pathologyM J E van Rijn, M J Bos, A Isaacs, et al.Genomics|September 16, 1999
Construction of a detailed physical and transcript map of the FTDP-17 candidate region on chromosome 17q21S Froelich, H Houlden, P Rizzu, et al.American Journal of Human Genetics|June 15, 2007
A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch populationFan Liu, Alejandro Arias-Vásquez, Kristel Sleegers, et al.Neurobiology of Disease|February 15, 2011
AFQ056, a new mGluR5 antagonist for treatment of fragile X syndromeJosien Levenga, Shigemi Hayashi, Femke M S de Vrij, et al.Pageof 51