Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

G A Danieli

Showing results (61-70 of 96) with videos related to

Pageof 10
Sort By:
Journal of Medical Genetics|February 1, 1992
Screening for mutations in the muscle promoter region and for exonic deletions in a series of 115 DMD and BMD patientsL Vitiello, M L Mostacciuolo, S Oliviero, et al.
Journal of Medical Genetics|November 1, 1994
Non-radioactive detection of 17p11.2 duplication in CMT1A: a study of 78 patientsF Schiavon, M L Mostacciuolo, F Saad, et al.
Human Mutation|January 1, 1993
A novel nonsense mutation in the human dystrophin geneF A Saad, G Vita, M Mora, et al.
Advances in Neurology|January 1, 1988
Heterogeneity of Charcot-Marie-Tooth disease suggested by a linkage studyG Micaglio, P Fardin, M Battilana, et al.
American Journal of Medical Genetics|March 1, 1994
Occurrence of two different intragenic deletions in two male relatives affected with Duchenne muscular dystrophyM L Mostacciuolo, M Miorin, L Vitiello, et al.
Biochemical and Biophysical Research Communications|January 13, 1997
Fine mapping of five human skeletal muscle genes: alpha-tropomyosin, beta-tropomyosin, troponin-I slow-twitch, troponin-I fast-twitch, and troponin-C fastN Tiso, L Rampoldi, A Pallavicini, et al.
The American Journal of Cardiology|November 15, 2000
Familial effort polymorphic ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy map to chromosome 1q42-43B Bauce, A Nava, A Rampazzo, et al.
Biochemical and Biophysical Research Communications|August 23, 1996
Chromosomal localization of the human genes, CPP32, Mch2, Mch3, and Ich-1, involved in cellular apoptosisN Tiso, A Pallavicini, T Muraro, et al.
Human Genetics|July 1, 1994
A study on duplications of the dystrophin gene: evidence of a geographical difference in the distribution of breakpoints by intronF Galvagni, F A Saad, G A Danieli, et al.
The International Journal of Artificial Organs|October 8, 2005
Hybrid test bench for evaluation of any device related to mechanical cardiac assistanceF M Colacino, M Arabia, G A Danieli, et al.
Pageof 10

Showing results (61-70 of 96) with videos related to

Sort By:
Pageof 10
Journal of Medical Genetics|February 1, 1992
Screening for mutations in the muscle promoter region and for exonic deletions in a series of 115 DMD and BMD patientsL Vitiello, M L Mostacciuolo, S Oliviero, et al.
Journal of Medical Genetics|November 1, 1994
Non-radioactive detection of 17p11.2 duplication in CMT1A: a study of 78 patientsF Schiavon, M L Mostacciuolo, F Saad, et al.
Human Mutation|January 1, 1993
A novel nonsense mutation in the human dystrophin geneF A Saad, G Vita, M Mora, et al.
Advances in Neurology|January 1, 1988
Heterogeneity of Charcot-Marie-Tooth disease suggested by a linkage studyG Micaglio, P Fardin, M Battilana, et al.
American Journal of Medical Genetics|March 1, 1994
Occurrence of two different intragenic deletions in two male relatives affected with Duchenne muscular dystrophyM L Mostacciuolo, M Miorin, L Vitiello, et al.
Biochemical and Biophysical Research Communications|January 13, 1997
Fine mapping of five human skeletal muscle genes: alpha-tropomyosin, beta-tropomyosin, troponin-I slow-twitch, troponin-I fast-twitch, and troponin-C fastN Tiso, L Rampoldi, A Pallavicini, et al.
The American Journal of Cardiology|November 15, 2000
Familial effort polymorphic ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy map to chromosome 1q42-43B Bauce, A Nava, A Rampazzo, et al.
Biochemical and Biophysical Research Communications|August 23, 1996
Chromosomal localization of the human genes, CPP32, Mch2, Mch3, and Ich-1, involved in cellular apoptosisN Tiso, A Pallavicini, T Muraro, et al.
Human Genetics|July 1, 1994
A study on duplications of the dystrophin gene: evidence of a geographical difference in the distribution of breakpoints by intronF Galvagni, F A Saad, G A Danieli, et al.
The International Journal of Artificial Organs|October 8, 2005
Hybrid test bench for evaluation of any device related to mechanical cardiac assistanceF M Colacino, M Arabia, G A Danieli, et al.
Pageof 10