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Journal of Hypertension|January 16, 2002
Different impact of deletion polymorphism of gene on the risk of renal and coronary artery diseaseOliviero Olivieri, Silvia Grazioli, Francesca Pizzolo, et al.
Clinical Chemistry and Laboratory Medicine|July 9, 2008
Genetic testing for adult-type hypolactasia in Italian familiesMonica Mottes, Francesca Belpinati, Monia Milani, et al.
Annals of Human Biology|September 4, 2010
Anthropological features of the CFTR gene: Its variability in an African populationBianca Maria Ciminelli, Cristina Bombieri, Cinzia Ciccacci, et al.
Molecular and Cellular Probes|December 2, 2009
Detection of a large deletion in the P-selectin (SELP) geneAlessandra Pasquali, Elisabetta Trabetti, Maria Grazia Romanelli, et al.
Clinical Chemistry|March 20, 2002
Biochemical and genetic markers of iron status and the risk of coronary artery disease: an angiography-based studyClaudia Bozzini, Domenico Girelli, Elisa Tinazzi, et al.
Journal of Lipid Research|October 18, 2003
Apolipoprotein C-III, metabolic syndrome, and risk of coronary artery diseaseOliviero Olivieri, Antonella Bassi, Chiara Stranieri, et al.
Clinical Chemistry and Laboratory Medicine|February 22, 2007
The Italian External Quality Control Programme for cystic fibrosis molecular diagnosis: 4 years of activityMarco Salvatore, Vincenzo Falbo, Giovanna Floridia, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemiaCristina Patuzzo, Carlo Castellani, Carlo Sagramoso, et al.
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