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

B T Darras

Showing results (1-10 of 55) with videos related to

Pageof 6
Sort By:
Clinics in Perinatology|December 13, 1997
Neuromuscular disorders in the newbornB T Darras
The Journal of Pediatrics|July 1, 1990
Molecular genetics of Duchenne and Becker muscular dystrophyB T Darras
Supplements to Clinical Neurophysiology|May 14, 2003
Role of EMG in the evaluation of presumed myopathies in the era of DNA analysisB T Darras
American Journal of Human Genetics|August 1, 1988
Myopathy in complex glycerol kinase deficiency patients is due to 3' deletions of the dystrophin geneB T Darras, U Francke
American Journal of Human Genetics|November 1, 1988
Normal human genomic restriction-fragment patterns and polymorphisms revealed by hybridization with the entire dystrophin cDNAB T Darras, U Francke
Nature|October 8, 1987
A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected maleB T Darras, U Francke
Neurological Research|March 1, 1992
Loss of heterozygosity on the short arm of chromosome 17 in human astrocytomasJ K Wu, B T Darras
Journal of Physics. Conference Series|July 30, 2013
Electrical impedance myography for the assessment of children with muscular dystrophy: a preliminary studyS B Rutkove, B T Darras
Pediatric Infectious Disease|July 1, 1983
Viral and bacterial pathogens of suspected sepsis in young infantsR J Leggiadro, B T Darras
Muscle & Nerve. Supplement|January 3, 2001
Acute care pediatric electromyographyH R Jones, B T Darras
Pageof 6

Showing results (1-10 of 55) with videos related to

Sort By:
Pageof 6
Clinics in Perinatology|December 13, 1997
Neuromuscular disorders in the newbornB T Darras
The Journal of Pediatrics|July 1, 1990
Molecular genetics of Duchenne and Becker muscular dystrophyB T Darras
Supplements to Clinical Neurophysiology|May 14, 2003
Role of EMG in the evaluation of presumed myopathies in the era of DNA analysisB T Darras
American Journal of Human Genetics|August 1, 1988
Myopathy in complex glycerol kinase deficiency patients is due to 3' deletions of the dystrophin geneB T Darras, U Francke
American Journal of Human Genetics|November 1, 1988
Normal human genomic restriction-fragment patterns and polymorphisms revealed by hybridization with the entire dystrophin cDNAB T Darras, U Francke
Nature|October 8, 1987
A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected maleB T Darras, U Francke
Neurological Research|March 1, 1992
Loss of heterozygosity on the short arm of chromosome 17 in human astrocytomasJ K Wu, B T Darras
Journal of Physics. Conference Series|July 30, 2013
Electrical impedance myography for the assessment of children with muscular dystrophy: a preliminary studyS B Rutkove, B T Darras
Pediatric Infectious Disease|July 1, 1983
Viral and bacterial pathogens of suspected sepsis in young infantsR J Leggiadro, B T Darras
Muscle & Nerve. Supplement|January 3, 2001
Acute care pediatric electromyographyH R Jones, B T Darras
Pageof 6