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

J Willems

Showing results (421-430 of 446) with videos related to

Pageof 45
Sort By:
Genomics|April 1, 1997
Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1pG Van Camp, P J Coucke, H Kunst, et al.
Journal of Medical Genetics|September 13, 2005
The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 geneK P Hoornaert, C Dewinter, I Vereecke, et al.
Human Molecular Genetics|June 9, 1998
Two frequent missense mutations in Pendred syndromeP Van Hauwe, L A Everett, P Coucke, et al.
Plant & Cell Physiology|January 9, 2018
Arabidopsis Phospholipase C3 is Involved in Lateral Root Initiation and ABA Responses in Seed Germination and Stomatal ClosureQianqian Zhang, Ringo van Wijk, Muhammad Shahbaz, et al.
American Journal of Human Genetics|May 11, 2005
Homozygous nonsense mutations in KIAA1279 are associated with malformations of the central and enteric nervous systemsAlice S Brooks, Aida M Bertoli-Avella, Grzegorz M Burzynski, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|November 22, 2008
Emergence and spread of vancomycin resistance among enterococci in EuropeG Werner, T M Coque, A M Hammerum, et al.
Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|October 18, 2024
Impact of serum neurofilament light on clinical decisions in a tertiary multiple sclerosis clinicZoë Ygj van Lierop, Mark Hj Wessels, Womei Ml Lekranty, et al.
Human Molecular Genetics|June 17, 1999
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 familiesP J Coucke, P Van Hauwe, P M Kelley, et al.
Neuromuscular Disorders : NMD|July 20, 2010
Myopathy with hexagonally cross-linked crystalloid inclusions: delineation of a clinico-pathological entityKristl G Claeys, Jean-François Pellissier, Federico Garcia-Bragado, et al.
Pageof 45

Showing results (421-430 of 446) with videos related to

Sort By:
Pageof 45
Genomics|April 1, 1997
Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1pG Van Camp, P J Coucke, H Kunst, et al.
Journal of Medical Genetics|September 13, 2005
The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 geneK P Hoornaert, C Dewinter, I Vereecke, et al.
Human Molecular Genetics|June 9, 1998
Two frequent missense mutations in Pendred syndromeP Van Hauwe, L A Everett, P Coucke, et al.
Plant & Cell Physiology|January 9, 2018
Arabidopsis Phospholipase C3 is Involved in Lateral Root Initiation and ABA Responses in Seed Germination and Stomatal ClosureQianqian Zhang, Ringo van Wijk, Muhammad Shahbaz, et al.
American Journal of Human Genetics|May 11, 2005
Homozygous nonsense mutations in KIAA1279 are associated with malformations of the central and enteric nervous systemsAlice S Brooks, Aida M Bertoli-Avella, Grzegorz M Burzynski, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|November 22, 2008
Emergence and spread of vancomycin resistance among enterococci in EuropeG Werner, T M Coque, A M Hammerum, et al.
Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|October 18, 2024
Impact of serum neurofilament light on clinical decisions in a tertiary multiple sclerosis clinicZoë Ygj van Lierop, Mark Hj Wessels, Womei Ml Lekranty, et al.
Human Molecular Genetics|June 17, 1999
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 familiesP J Coucke, P Van Hauwe, P M Kelley, et al.
Neuromuscular Disorders : NMD|July 20, 2010
Myopathy with hexagonally cross-linked crystalloid inclusions: delineation of a clinico-pathological entityKristl G Claeys, Jean-François Pellissier, Federico Garcia-Bragado, et al.
Pageof 45