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Clinical Genetics|March 30, 2011
A novel g.-1258G>A mutation in a conserved putative regulatory element of PAX9 is associated with autosomal dominant molar hypodontiaG A Mendoza-Fandino, J M Gee, S Ben-Dor, et al.American Journal of Human Genetics|April 17, 1999
Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levelsP Pajukanta, J D Terwilliger, M Perola, et al.Pageof 10