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Molecular and Cellular Probes|April 1, 1995
Homozygosity for a novel splice site mutation (2790-2 A--->G) preceding exon 15 of the CFTR gene in a cystic fibrosis patient of North-East Italian descentC Marigo, C Bombieri, L Bisceglia, et al.Journal of Medical Genetics|November 1, 1990
Pancreatic function and gene deletion F508 in cystic fibrosisG Borgo, G Mastella, P Gasparini, et al.Biochemistry|April 6, 1976
Characterization of the gamma subunits of the 7S nerve growth factor complexR W Stach, A C Server, P F Pignatti, et al.Recenti Progressi in Medicina|January 1, 1990
Search of HIV DNA by polymerase chain reaction in the urine sediments of seropositive individualsP Gasparini, A Savoia, P F Pignatti, et al.Molecular and Cellular Probes|December 1, 1996
A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1)E Bresin, S Rossetti, S Englisch, et al.International Journal of Immunogenetics|November 16, 2007
Two new highly polymorphic markers in the 3' UTR region of the PLA2G7 geneM Gomez Lira, L Provezza, C Terranova, et al.Molecular and Cellular Probes|March 17, 1998
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A geneC Perusi, M Gomez-Lira, M Mottes, et al.Headache|March 31, 2001
Frequency of factor V Leiden in juvenile migraine with auraS Soriani, C Borgna-Pignatti, E Trabetti, et al.Molecular and Cellular Probes|June 1, 1995
Allele and genotype frequencies of eight DNA polymorphisms in the Italian populationE Trabetti, R Galavotti, A Casartelli, et al.ESMO Open|March 18, 2021
The European Medicines Agency review of entrectinib for the treatment of adult or paediatric patients with solid tumours who have a neurotrophic tyrosine receptor kinase gene fusions and adult patients with non-small-cell lung cancer harbouring ROS1 rearrangementsJ Delgado, E Pean, D Melchiorri, et al.Pageof 15