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

Andrew Orr

Showing results (21-30 of 26) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 26 results.
Nature Genetics|March 2, 2011
Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndromeDuane L Guernsey, Makoto Matsuoka, Haiyan Jiang, et al.
American Journal of Human Genetics|July 6, 2010
Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4Duane L Guernsey, Haiyan Jiang, Julie Hussin, et al.
Plos Genetics|October 24, 2014
Germline mutations in MAP3K6 are associated with familial gastric cancerDaniel Gaston, Samantha Hansford, Carla Oliveira, et al.
Science Advances|February 25, 2021
Spatial heterogeneity and environmental predictors of permafrost region soil organic carbon stocksUmakant Mishra, Gustaf Hugelius, Eitan Shelef, et al.
Kidney International|December 14, 2023
Autosomal dominant ApoA4 mutations present as tubulointerstitial kidney disease with medullary amyloidosisTereza Kmochová, Kendrah O Kidd, Andrew Orr, et al.
JAMA|February 23, 2021
Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye, Zheng Li, Zhenxun Wang, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Nature Genetics|March 2, 2011
Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndromeDuane L Guernsey, Makoto Matsuoka, Haiyan Jiang, et al.
American Journal of Human Genetics|July 6, 2010
Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4Duane L Guernsey, Haiyan Jiang, Julie Hussin, et al.
Plos Genetics|October 24, 2014
Germline mutations in MAP3K6 are associated with familial gastric cancerDaniel Gaston, Samantha Hansford, Carla Oliveira, et al.
Science Advances|February 25, 2021
Spatial heterogeneity and environmental predictors of permafrost region soil organic carbon stocksUmakant Mishra, Gustaf Hugelius, Eitan Shelef, et al.
Kidney International|December 14, 2023
Autosomal dominant ApoA4 mutations present as tubulointerstitial kidney disease with medullary amyloidosisTereza Kmochová, Kendrah O Kidd, Andrew Orr, et al.
JAMA|February 23, 2021
Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye, Zheng Li, Zhenxun Wang, et al.
Pageof 3