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

Donald F Conrad

Showing results (101-110 of 106) with videos related to

Pageof 11
Sort By:
You have reached the last page of results.This site can display upto 106 results.
Nature Communications|December 26, 2022
Diverse monogenic subforms of human spermatogenic failureLiina Nagirnaja, Alexandra M Lopes, Wu-Lin Charng, et al.
Science (New York, N.Y.)|February 21, 2012
A systematic survey of loss-of-function variants in human protein-coding genesDaniel G MacArthur, Suganthi Balasubramanian, Adam Frankish, et al.
Nature Communications|November 26, 2020
The genetic architecture of sporadic and multiple consecutive miscarriageTriin Laisk, Ana Luiza G Soares, Teresa Ferreira, et al.
HGG Advances|February 1, 2024
Heterozygous loss-of-function SMC3 variants are associated with variable growth and developmental featuresMorad Ansari, Kamli N W Faour, Akiko Shimamura, et al.
Nature|February 5, 2011
Mapping copy number variation by population-scale genome sequencingRyan E Mills, Klaudia Walter, Chip Stewart, et al.
Nature|April 3, 2010
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls, Nick Craddock, Matthew E Hurles, et al.
Pageof 11

Showing results (101-110 of 106) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 106 results.
Nature Communications|December 26, 2022
Diverse monogenic subforms of human spermatogenic failureLiina Nagirnaja, Alexandra M Lopes, Wu-Lin Charng, et al.
Science (New York, N.Y.)|February 21, 2012
A systematic survey of loss-of-function variants in human protein-coding genesDaniel G MacArthur, Suganthi Balasubramanian, Adam Frankish, et al.
Nature Communications|November 26, 2020
The genetic architecture of sporadic and multiple consecutive miscarriageTriin Laisk, Ana Luiza G Soares, Teresa Ferreira, et al.
HGG Advances|February 1, 2024
Heterozygous loss-of-function SMC3 variants are associated with variable growth and developmental featuresMorad Ansari, Kamli N W Faour, Akiko Shimamura, et al.
Nature|February 5, 2011
Mapping copy number variation by population-scale genome sequencingRyan E Mills, Klaudia Walter, Chip Stewart, et al.
Nature|April 3, 2010
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls, Nick Craddock, Matthew E Hurles, et al.
Pageof 11