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G A Danieli

Showing results (31-40 of 96) with videos related to

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Journal of Medical Genetics|June 1, 1991
Segregation and sporadic cases in families with Hunter's syndromeG Machill, G Barbujani, G A Danieli, et al.
Medical Engineering & Physics|October 24, 2006
Modeling, analysis, and validation of a pneumatically driven left ventricle for use in mock circulatory systemsF M Colacino, M Arabia, F Moscato, et al.
Human Molecular Genetics|June 1, 1994
DXS997 localized to intron 48 of dystrophinF A Saad, C Busque, L Vitiello, et al.
American Journal of Medical Genetics|November 7, 1998
Double missense mutation in exon 41 of the human dystrophin gene detected by double strand conformation analysisF A Saad, L Merlini, M L Mostacciuolo, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Prevalence of dystrophin-positive fibers in 85 Duchenne muscular dystrophy patientsM Fanin, G A Danieli, L Vitiello, et al.
Genomics|November 5, 1997
Exon-intron organization of the human dystrophin geneC Nobile, J Marchi, V Nigro, et al.
Human Genetics|January 1, 1980
Duchenne muscular dystrophy: data from family studiesG A Danieli, M L Mostacciuolo, G Pilotto, et al.
Gene|December 31, 1997
Conservation of a putative AP1 binding site and complete homology to a fetal brain EST in a region upstream of the core muscle promoter in the human dystrophin geneT Patarnello, H J Klamut, G A Danieli, et al.
Forensic Science International|December 4, 2001
Italian population data for D1S1656, D3S1358, D8S1132, D10S2325, VWA, FES/FPS, and F13A01D De Leo, S Turrina, M Marigo, et al.
Neuroepidemiology|January 1, 1992
Epidemiology of spinal muscular atrophies in a sample of the Italian populationM L Mostacciuolo, G A Danieli, C Trevisan, et al.
Pageof 10

Showing results (31-40 of 96) with videos related to

Sort By:
Pageof 10
Journal of Medical Genetics|June 1, 1991
Segregation and sporadic cases in families with Hunter's syndromeG Machill, G Barbujani, G A Danieli, et al.
Medical Engineering & Physics|October 24, 2006
Modeling, analysis, and validation of a pneumatically driven left ventricle for use in mock circulatory systemsF M Colacino, M Arabia, F Moscato, et al.
Human Molecular Genetics|June 1, 1994
DXS997 localized to intron 48 of dystrophinF A Saad, C Busque, L Vitiello, et al.
American Journal of Medical Genetics|November 7, 1998
Double missense mutation in exon 41 of the human dystrophin gene detected by double strand conformation analysisF A Saad, L Merlini, M L Mostacciuolo, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Prevalence of dystrophin-positive fibers in 85 Duchenne muscular dystrophy patientsM Fanin, G A Danieli, L Vitiello, et al.
Genomics|November 5, 1997
Exon-intron organization of the human dystrophin geneC Nobile, J Marchi, V Nigro, et al.
Human Genetics|January 1, 1980
Duchenne muscular dystrophy: data from family studiesG A Danieli, M L Mostacciuolo, G Pilotto, et al.
Gene|December 31, 1997
Conservation of a putative AP1 binding site and complete homology to a fetal brain EST in a region upstream of the core muscle promoter in the human dystrophin geneT Patarnello, H J Klamut, G A Danieli, et al.
Forensic Science International|December 4, 2001
Italian population data for D1S1656, D3S1358, D8S1132, D10S2325, VWA, FES/FPS, and F13A01D De Leo, S Turrina, M Marigo, et al.
Neuroepidemiology|January 1, 1992
Epidemiology of spinal muscular atrophies in a sample of the Italian populationM L Mostacciuolo, G A Danieli, C Trevisan, et al.
Pageof 10