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Molecular and Cellular Probes|April 1, 1995
Identification of six novel CFTR mutations in a sample of Italian cystic fibrosis patientsC Férec, G Novelli, C Verlingue, et al.
Neurology|June 16, 2005
The PINK1 phenotype can be indistinguishable from idiopathic Parkinson diseaseA Albanese, E M Valente, L M Romito, et al.
Cytogenetic and Genome Research|August 17, 2005
Pure trisomy 19p syndrome in an infant with an extra ring chromosomeA Novelli, C Ceccarini, L Bernardini, et al.
Biochemistry and Molecular Biology International|October 27, 2009
Recombinant CTFR detection in CF tracheal epithelial cells following in vitro liposomeme-mediated gene transferA Colosimo, S Scarpino, F Sangiuolo, et al.
Human Heredity|September 1, 1993
Identification of three novel cystic fibrosis mutations in a sample of Italian cystic fibrosis patientsM P Audrézet, G Novelli, B Mercier, et al.
Clinical and Experimental Rheumatology|April 22, 2010
A novel homozygous splice site mutation in the HPGD gene causes mild primary hypertrophic osteoarthropathyL Sinibaldi, G Harifi, I Bottillo, et al.
The Science of the Total Environment|June 1, 2020
Connectivity and hydrological efficiency dynamics at active volcanoes, MexicoA J Ortíz-Rodríguez, L Capra, C Muñoz-Robles, et al.
Journal of Pediatric Surgery|October 3, 2006
Approach to diagnosis and treatment of pediatric primary tumors of the diaphragmMichaela Cada, J Ted Gerstle, Jeffrey Traubici, et al.
Neuromuscular Disorders : NMD|July 10, 1999
Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patientsM Gennarelli, M Pavoni, P Amicucci, et al.
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