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

M A Levenstien

Showing results (1-10 of 4) with videos related to

Pageof 1
Sort By:
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|February 27, 2003
Errors and linkage disequilibrium interact multiplicatively when computing sample sizes for genetic case-control association studiesD Gordon, M A Levenstien, S J Finch, et al.
Genetic Epidemiology|January 17, 2002
Two approaches for consolidating results from genome scans of complex traits: selection methods and scan statisticsD Gordon, J Hoh, S J Finch, et al.
JAMA|July 13, 2000
Mapping of a gene for severe pediatric gastroesophageal reflux to chromosome 13q14F Z Hu, R A Preston, J C Post, et al.
Molecular Genetics and Metabolism|December 26, 2001
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementiaM J Kovach, B Waggoner, S M Leal, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|February 27, 2003
Errors and linkage disequilibrium interact multiplicatively when computing sample sizes for genetic case-control association studiesD Gordon, M A Levenstien, S J Finch, et al.
Genetic Epidemiology|January 17, 2002
Two approaches for consolidating results from genome scans of complex traits: selection methods and scan statisticsD Gordon, J Hoh, S J Finch, et al.
JAMA|July 13, 2000
Mapping of a gene for severe pediatric gastroesophageal reflux to chromosome 13q14F Z Hu, R A Preston, J C Post, et al.
Molecular Genetics and Metabolism|December 26, 2001
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementiaM J Kovach, B Waggoner, S M Leal, et al.
Pageof 1