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G A Danieli

Showing results (21-30 of 96) with videos related to

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Human Genetics|March 30, 2004
Gene symbol: RYR2. Disease: Effort-induced polymorphic ventricular arrhythmiasC Veronese, A Bagattin, A Rampazzo, et al.
Genome Research|March 18, 2000
The human adult skeletal muscle transcriptional profile reconstructed by a novel computational approachS Bortoluzzi, F d'Alessi, C Romualdi, et al.
Bioinformatics (Oxford, England)|December 26, 2001
Differential expression of genes coding for ribosomal proteins in different human tissuesS Bortoluzzi, F d'Alessi, C Romualdi, et al.
Human Genetics|March 30, 2004
Gene symbol: RYR2. Disease: Effort-induced polymorphic ventricular arrhythmiasA Bagattin, C Veronese, A Rampazzo, et al.
Minerva Pediatrica|August 31, 1986
[Genetic counseling in hereditary neuromuscular diseases]G A Danieli, M L Mostacciuolo, P Marchesini, et al.
Human Genetics|February 11, 1977
Duchenne muscular dystrophy. A population studyG A Danieli, M L Mostacciuolo, A Bonfante, et al.
American Journal of Medical Genetics|June 15, 1991
Genetic epidemiology of hereditary motor sensory neuropathies (type I)M L Mostacciuolo, G Micaglio, P Fardin, et al.
Human Molecular Genetics|December 1, 1993
DXS997 localized to intron 48 of dystrophinF A Saad, C Busque, L Vitiello, et al.
Neuromuscular Disorders : NMD|July 1, 1994
A possible missense mutation detected in the dystrophin gene by Double-Strand Conformation Analysis (DSCA)F A Saad, G Vita, L Toffolatti, et al.
American Journal of Medical Genetics|March 1, 1989
Problems in genetic counseling in a family with an "atypical" centronuclear myopathyB Müller, M L Mostacciuolo, G A Danieli, et al.
Pageof 10

Showing results (21-30 of 96) with videos related to

Sort By:
Pageof 10
Human Genetics|March 30, 2004
Gene symbol: RYR2. Disease: Effort-induced polymorphic ventricular arrhythmiasC Veronese, A Bagattin, A Rampazzo, et al.
Genome Research|March 18, 2000
The human adult skeletal muscle transcriptional profile reconstructed by a novel computational approachS Bortoluzzi, F d'Alessi, C Romualdi, et al.
Bioinformatics (Oxford, England)|December 26, 2001
Differential expression of genes coding for ribosomal proteins in different human tissuesS Bortoluzzi, F d'Alessi, C Romualdi, et al.
Human Genetics|March 30, 2004
Gene symbol: RYR2. Disease: Effort-induced polymorphic ventricular arrhythmiasA Bagattin, C Veronese, A Rampazzo, et al.
Minerva Pediatrica|August 31, 1986
[Genetic counseling in hereditary neuromuscular diseases]G A Danieli, M L Mostacciuolo, P Marchesini, et al.
Human Genetics|February 11, 1977
Duchenne muscular dystrophy. A population studyG A Danieli, M L Mostacciuolo, A Bonfante, et al.
American Journal of Medical Genetics|June 15, 1991
Genetic epidemiology of hereditary motor sensory neuropathies (type I)M L Mostacciuolo, G Micaglio, P Fardin, et al.
Human Molecular Genetics|December 1, 1993
DXS997 localized to intron 48 of dystrophinF A Saad, C Busque, L Vitiello, et al.
Neuromuscular Disorders : NMD|July 1, 1994
A possible missense mutation detected in the dystrophin gene by Double-Strand Conformation Analysis (DSCA)F A Saad, G Vita, L Toffolatti, et al.
American Journal of Medical Genetics|March 1, 1989
Problems in genetic counseling in a family with an "atypical" centronuclear myopathyB Müller, M L Mostacciuolo, G A Danieli, et al.
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