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R Giorda

Showing results (51-60 of 60) with videos related to

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Clinical Genetics|April 24, 2010
Refining the phenotype associated with MEF2C haploinsufficiencyF Novara, S Beri, R Giorda, et al.
Genes, Brain, and Behavior|August 31, 2006
Effect of the catechol-O-methyltransferase val(158)met genotype on children's early phases of facial stimuli processingM Battaglia, A Zanoni, R Giorda, et al.
Epidemiology and Psychiatric Sciences|October 24, 2013
Effect of the serotonin transporter gene and of environment on the continuity of anxiety and depression traits throughout adolescenceM Nobile, A Greco, G Perna, et al.
Molecular Syndromology|March 5, 2011
Olfactory Receptor-Related Duplicons Mediate a Microdeletion at 11q13.2q13.4 Associated with a Syndromic PhenotypeA Wischmeijer, P Magini, R Giorda, et al.
Genes, Brain, and Behavior|November 27, 2012
An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypesS Mascheretti, A Bureau, M Battaglia, et al.
Neuromuscular Disorders : NMD|May 23, 2001
Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuriaR Cagliani, G P Comi, L Tancredi, et al.
Neuromuscular Disorders : NMD|December 18, 2003
Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian populationR Cagliani, F Fortunato, R Giorda, et al.
Journal of Medical Genetics|June 3, 2004
Selective disruption of muscle and brain-specific BPAG1 isoforms in a girl with a 6;15 translocation, cognitive and motor delay, and tracheo-oesophageal atresiaR Giorda, A Cerritello, M C Bonaglia, et al.
American Journal of Human Genetics|March 7, 2001
Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangementsS Giglio, K W Broman, N Matsumoto, et al.
American Journal of Human Genetics|September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disordersB Wissinger, D Gamer, H Jägle, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Clinical Genetics|April 24, 2010
Refining the phenotype associated with MEF2C haploinsufficiencyF Novara, S Beri, R Giorda, et al.
Genes, Brain, and Behavior|August 31, 2006
Effect of the catechol-O-methyltransferase val(158)met genotype on children's early phases of facial stimuli processingM Battaglia, A Zanoni, R Giorda, et al.
Epidemiology and Psychiatric Sciences|October 24, 2013
Effect of the serotonin transporter gene and of environment on the continuity of anxiety and depression traits throughout adolescenceM Nobile, A Greco, G Perna, et al.
Molecular Syndromology|March 5, 2011
Olfactory Receptor-Related Duplicons Mediate a Microdeletion at 11q13.2q13.4 Associated with a Syndromic PhenotypeA Wischmeijer, P Magini, R Giorda, et al.
Genes, Brain, and Behavior|November 27, 2012
An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypesS Mascheretti, A Bureau, M Battaglia, et al.
Neuromuscular Disorders : NMD|May 23, 2001
Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuriaR Cagliani, G P Comi, L Tancredi, et al.
Neuromuscular Disorders : NMD|December 18, 2003
Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian populationR Cagliani, F Fortunato, R Giorda, et al.
Journal of Medical Genetics|June 3, 2004
Selective disruption of muscle and brain-specific BPAG1 isoforms in a girl with a 6;15 translocation, cognitive and motor delay, and tracheo-oesophageal atresiaR Giorda, A Cerritello, M C Bonaglia, et al.
American Journal of Human Genetics|March 7, 2001
Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangementsS Giglio, K W Broman, N Matsumoto, et al.
American Journal of Human Genetics|September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disordersB Wissinger, D Gamer, H Jägle, et al.
Pageof 6