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

Nature genetics

Showing results (141-150 of 10,142) with videos related to

Pageof 1,015
Sort By:
Nature Genetics|June 10, 1998
Positional cloning of the gene for Nijmegen breakage syndromeS Matsuura, H Tauchi, A Nakamura, et al.
Nature Genetics|July 26, 2016
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosisWouter van Rheenen, Aleksey Shatunov, Annelot M Dekker, et al.
Nature Genetics|January 13, 1998
Turning on the centromereK H Choo
Nature Genetics|January 13, 1998
Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCRA Martínez-Mir, E Paloma, R Allikmets, et al.
Nature Genetics|January 13, 1998
No female embryonic lethality in mice nullizygous for Msh2 and p53N J Toft, M J Arends, A H Wyllie, et al.
Nature Genetics|January 13, 1998
Hippocratic or hypocritic: birth pangs of an ethical codeN E Morton
Nature Genetics|January 13, 1998
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newbornsN A Singh, C Charlier, D Stauffer, et al.
Nature Genetics|January 13, 1998
Association of a human G-protein beta3 subunit variant with hypertensionW Siffert, D Rosskopf, G Siffert, et al.
Nature Genetics|January 13, 1998
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy familyC Charlier, N A Singh, S G Ryan, et al.
Nature Genetics|March 21, 1998
Getting hip to the chip
Pageof 1,015

Showing results (141-150 of 10,142) with videos related to

Sort By:
Pageof 1,015
Nature Genetics|June 10, 1998
Positional cloning of the gene for Nijmegen breakage syndromeS Matsuura, H Tauchi, A Nakamura, et al.
Nature Genetics|July 26, 2016
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosisWouter van Rheenen, Aleksey Shatunov, Annelot M Dekker, et al.
Nature Genetics|January 13, 1998
Turning on the centromereK H Choo
Nature Genetics|January 13, 1998
Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCRA Martínez-Mir, E Paloma, R Allikmets, et al.
Nature Genetics|January 13, 1998
No female embryonic lethality in mice nullizygous for Msh2 and p53N J Toft, M J Arends, A H Wyllie, et al.
Nature Genetics|January 13, 1998
Hippocratic or hypocritic: birth pangs of an ethical codeN E Morton
Nature Genetics|January 13, 1998
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newbornsN A Singh, C Charlier, D Stauffer, et al.
Nature Genetics|January 13, 1998
Association of a human G-protein beta3 subunit variant with hypertensionW Siffert, D Rosskopf, G Siffert, et al.
Nature Genetics|January 13, 1998
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy familyC Charlier, N A Singh, S G Ryan, et al.
Nature Genetics|March 21, 1998
Getting hip to the chip
Pageof 1,015