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G A Danieli

Showing results (41-50 of 96) with videos related to

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Journal of Forensic Sciences|February 24, 2001
Allele frequency distributions for D1S1656, D8S1132, D10S2325, D18S51, and D21S11 loci in a north Italy populationS Turrina, D De Leo, M Marigo, et al.
Human Genetics|November 1, 1992
Further evidence of a duplication in 17p11.2 in families with recurrence of HMSN Ia (Charcot-Marie-Tooth neuropathy type Ia)E Müller, M L Mostacciuolo, G Micaglio, et al.
Genetic Epidemiology|January 1, 1987
Genetic epidemiology of myotonic dystrophyM L Mostacciuolo, G Barbujani, M Armani, et al.
Human Genetics|March 1, 1987
Population data on benign and severe forms of X-linked muscular dystrophyM L Mostacciuolo, A Lombardi, V Cambissa, et al.
Muscle & Nerve|October 1, 1995
Dystrophin-positive fibers in Duchenne dystrophy: origin and correlation to clinical courseM Fanin, G A Danieli, M Cadaldini, et al.
Cardiologia (Rome, Italy)|April 1, 1983
[Familial incidence and modes of inheritance of hypertrophic cardiomyopathy. Genetic analysis of several families]P Stritoni, G Fasoli, G M Boffa, et al.
PCR Methods and Applications|August 1, 1993
Detection of unknown gene mutations by multiplex single-strand conformation polymorphism (MSSCP)F A Saad, L Vitiello, S Oliviero, et al.
Human Genetics|March 30, 2004
Gene symbol: RYR2. Disease: Arrhythmogenic right ventricular cardiomyopathy type 2N Tiso, B Bauce, A Rampazzo, et al.
Human Genetics|March 30, 2004
Gene symbol: RYR2. Disease: Effort-induced polymorphic ventricular arrhythmiasA Bagattin, B Bauce, A Rampazzo, et al.
American Journal of Medical Genetics|October 2, 1996
Mutation analysis in Duchenne and Becker muscular dystrophy patients from Bulgaria shows a peculiar distribution of breakpoints by intronA Todoroya, J Bronzova, M Miorin, et al.
Pageof 10

Showing results (41-50 of 96) with videos related to

Sort By:
Pageof 10
Journal of Forensic Sciences|February 24, 2001
Allele frequency distributions for D1S1656, D8S1132, D10S2325, D18S51, and D21S11 loci in a north Italy populationS Turrina, D De Leo, M Marigo, et al.
Human Genetics|November 1, 1992
Further evidence of a duplication in 17p11.2 in families with recurrence of HMSN Ia (Charcot-Marie-Tooth neuropathy type Ia)E Müller, M L Mostacciuolo, G Micaglio, et al.
Genetic Epidemiology|January 1, 1987
Genetic epidemiology of myotonic dystrophyM L Mostacciuolo, G Barbujani, M Armani, et al.
Human Genetics|March 1, 1987
Population data on benign and severe forms of X-linked muscular dystrophyM L Mostacciuolo, A Lombardi, V Cambissa, et al.
Muscle & Nerve|October 1, 1995
Dystrophin-positive fibers in Duchenne dystrophy: origin and correlation to clinical courseM Fanin, G A Danieli, M Cadaldini, et al.
Cardiologia (Rome, Italy)|April 1, 1983
[Familial incidence and modes of inheritance of hypertrophic cardiomyopathy. Genetic analysis of several families]P Stritoni, G Fasoli, G M Boffa, et al.
PCR Methods and Applications|August 1, 1993
Detection of unknown gene mutations by multiplex single-strand conformation polymorphism (MSSCP)F A Saad, L Vitiello, S Oliviero, et al.
Human Genetics|March 30, 2004
Gene symbol: RYR2. Disease: Arrhythmogenic right ventricular cardiomyopathy type 2N Tiso, B Bauce, A Rampazzo, et al.
Human Genetics|March 30, 2004
Gene symbol: RYR2. Disease: Effort-induced polymorphic ventricular arrhythmiasA Bagattin, B Bauce, A Rampazzo, et al.
American Journal of Medical Genetics|October 2, 1996
Mutation analysis in Duchenne and Becker muscular dystrophy patients from Bulgaria shows a peculiar distribution of breakpoints by intronA Todoroya, J Bronzova, M Miorin, et al.
Pageof 10