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

Neurology. Genetics

Showing results (381-390 of 1,012) with videos related to

Pageof 102
Sort By:
Neurology. Genetics|April 12, 2016
Genetic analysis for a shared biological basis between migraine and coronary artery diseaseBendik S Winsvold, Christopher P Nelson, Rainer Malik, et al.
Neurology. Genetics|April 12, 2016
Welcome to Neurology: GeneticsStefan M Pulst
Neurology. Genetics|April 12, 2016
PFKM gene defect and glycogen storage disease GSDVII with misleading enzyme histochemistryMari Auranen, Johanna Palmio, Emil Ylikallio, et al.
Neurology. Genetics|April 12, 2016
A novel DYNC1H1 mutation causing spinal muscular atrophy with lower extremity predominanceQi Niu, Xingxia Wang, Mingchao Shi, et al.
Neurology. Genetics|April 29, 2016
Analysis of rare copy number variation in absence epilepsiesLaura Addis, Richard E Rosch, Antonio Valentin, et al.
Neurology. Genetics|April 29, 2016
Compound heterozygote mutations in SPG7 in a family with adult-onset primary lateral sclerosisYi Yang, Lei Zhang, David R Lynch, et al.
Neurology. Genetics|April 29, 2016
Exonic deletion of SLC9A9 in autism with epilepsyMeeta Cardon, Karen D Evankovich, J Lloyd Holder
Neurology. Genetics|April 29, 2016
Copy number variants in absence epilepsy: Further complications of the pictureChantal Depondt
Neurology. Genetics|April 29, 2016
Parkinson disease (PARK) genes are somatically mutated in cutaneous melanomaRivka Inzelberg, Yardena Samuels, Esther Azizi, et al.
Neurology. Genetics|April 12, 2016
Mutation in PNKP presenting initially as axonal Charcot-Marie-Tooth diseaseJosé Luiz Pedroso, Clarissa R R Rocha, Lucia I Macedo-Souza, et al.
Pageof 102

Showing results (381-390 of 1,012) with videos related to

Sort By:
Pageof 102
Neurology. Genetics|April 12, 2016
Genetic analysis for a shared biological basis between migraine and coronary artery diseaseBendik S Winsvold, Christopher P Nelson, Rainer Malik, et al.
Neurology. Genetics|April 12, 2016
Welcome to Neurology: GeneticsStefan M Pulst
Neurology. Genetics|April 12, 2016
PFKM gene defect and glycogen storage disease GSDVII with misleading enzyme histochemistryMari Auranen, Johanna Palmio, Emil Ylikallio, et al.
Neurology. Genetics|April 12, 2016
A novel DYNC1H1 mutation causing spinal muscular atrophy with lower extremity predominanceQi Niu, Xingxia Wang, Mingchao Shi, et al.
Neurology. Genetics|April 29, 2016
Analysis of rare copy number variation in absence epilepsiesLaura Addis, Richard E Rosch, Antonio Valentin, et al.
Neurology. Genetics|April 29, 2016
Compound heterozygote mutations in SPG7 in a family with adult-onset primary lateral sclerosisYi Yang, Lei Zhang, David R Lynch, et al.
Neurology. Genetics|April 29, 2016
Exonic deletion of SLC9A9 in autism with epilepsyMeeta Cardon, Karen D Evankovich, J Lloyd Holder
Neurology. Genetics|April 29, 2016
Copy number variants in absence epilepsy: Further complications of the pictureChantal Depondt
Neurology. Genetics|April 29, 2016
Parkinson disease (PARK) genes are somatically mutated in cutaneous melanomaRivka Inzelberg, Yardena Samuels, Esther Azizi, et al.
Neurology. Genetics|April 12, 2016
Mutation in PNKP presenting initially as axonal Charcot-Marie-Tooth diseaseJosé Luiz Pedroso, Clarissa R R Rocha, Lucia I Macedo-Souza, et al.
Pageof 102