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European Journal of Human Genetics : EJHG|January 1, 1994
Further localization of the gene for hereditary paragangliomas and evidence for linkage in unrelated familiesP Heutink, E M van Schothorst, A G van der Mey, et al.
Virchows Archiv : an International Journal of Pathology|February 24, 2001
Absence of a PDX-1 mutation and normal gastroduodenal immunohistology in a child with pancreatic agenesisA M Verwest, M Poelman, W N Dinjens, et al.
Investigative Ophthalmology & Visual Science|May 8, 2009
Association of cognitive functioning with retinal nerve fiber layer thicknessLeonieke M E van Koolwijk, Dominiek D G Despriet, Cornelia M Van Duijn, et al.
Diabetes|August 13, 2008
Predicting type 2 diabetes based on polymorphisms from genome-wide association studies: a population-based studyMandy van Hoek, Abbas Dehghan, Jacqueline C M Witteman, et al.
Genes, Brain, and Behavior|January 20, 2012
The effect of an mGluR5 inhibitor on procedural memory and avoidance discrimination impairments in Fmr1 KO miceM F Vinueza Veloz, R A M Buijsen, R Willemsen, et al.
American Journal of Human Genetics|November 1, 1994
Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular dataB C Hamel, A P Smits, E de Graaff, et al.
Diabetes|March 2, 2002
A genome-wide search for linkage-disequilibrium with type 1 diabetes in a recent genetically isolated population from the NetherlandsNorbert Vaessen, Peter Heutink, Jeanine J Houwing-Duistermaat, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 15, 2013
Risk scores of common genetic variants for lipid levels influence atherosclerosis and incident coronary heart diseaseAaron Isaacs, Sara M Willems, Daniel Bos, et al.
European Journal of Cardiovascular Prevention and Rehabilitation : Official Journal of the European Society of Cardiology, Working Groups on Epidemiology & Prevention and Cardiac Rehabilitation and Exercise Physiology|June 15, 2007
The cholesteryl ester transfer protein I405V polymorphism is associated with increased high-density lipoprotein levels and decreased risk of myocardial infarction: the Rotterdam StudyAaron Isaacs, Fakhredin A Sayed-Tabatabaei, Albert Hofman, et al.
American Journal of Medical Genetics|July 15, 1994
DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 geneA M van den Ouweland, B B de Vries, P L Bakker, et al.
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