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

A MacRae

Showing results (561-570 of 599) with videos related to

Pageof 60
Sort By:
Lancet (London, England)|December 28, 2014
Crohn's disease management after intestinal resection: a randomised trialPeter De Cruz, Michael A Kamm, Amy L Hamilton, et al.
Cancers|October 28, 2023
DNA Mismatch Repair Gene Variant Classification: Evaluating the Utility of Somatic Mutations and Mismatch Repair Deficient Colonic Crypts and Endometrial GlandsRomy Walker, Khalid Mahmood, Julia Como, et al.
Nature Genetics|December 4, 2023
Perturbational phenotyping of human blood cells reveals genetically determined latent traits associated with subsets of common diseasesMax Homilius, Wandi Zhu, Samuel S Eddy, et al.
European Heart Journal|January 15, 2009
Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillationStefan Kääb, Dawood Darbar, Charlotte van Noord, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 10, 2015
PMS2 monoallelic mutation carriers: the known unknownMcKinsey L Goodenberger, Brittany C Thomas, Douglas Riegert-Johnson, et al.
Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Systematic large-scale application of ClinGen InSiGHT <i>APC</i> -specific ACMG/AMP variant classification criteria substantially alleviates the burden of variants of uncertain significance in ClinVar and LOVD databasesXiaoyu Yin, Marcy Richardson, Andreas Laner, et al.
Science (New York, N.Y.)|November 8, 2008
GENETICS. The Human Variome ProjectRichard G H Cotton, Arleen D Auerbach, Myles Axton, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 11, 2010
Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the colon cancer family registryMichael D Walsh, Daniel D Buchanan, Margaret C Cummings, et al.
American Journal of Human Genetics|November 28, 2002
The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish populationW D Foulkes, I Thiffault, S B Gruber, et al.
Journal of Crohn'S & Colitis|April 10, 2015
Effect of intestinal resection on quality of life in Crohn's diseaseEmily K Wright, Michael A Kamm, Peter De Cruz, et al.
Pageof 60

Showing results (561-570 of 599) with videos related to

Sort By:
Pageof 60
Lancet (London, England)|December 28, 2014
Crohn's disease management after intestinal resection: a randomised trialPeter De Cruz, Michael A Kamm, Amy L Hamilton, et al.
Cancers|October 28, 2023
DNA Mismatch Repair Gene Variant Classification: Evaluating the Utility of Somatic Mutations and Mismatch Repair Deficient Colonic Crypts and Endometrial GlandsRomy Walker, Khalid Mahmood, Julia Como, et al.
Nature Genetics|December 4, 2023
Perturbational phenotyping of human blood cells reveals genetically determined latent traits associated with subsets of common diseasesMax Homilius, Wandi Zhu, Samuel S Eddy, et al.
European Heart Journal|January 15, 2009
Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillationStefan Kääb, Dawood Darbar, Charlotte van Noord, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 10, 2015
PMS2 monoallelic mutation carriers: the known unknownMcKinsey L Goodenberger, Brittany C Thomas, Douglas Riegert-Johnson, et al.
Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Systematic large-scale application of ClinGen InSiGHT <i>APC</i> -specific ACMG/AMP variant classification criteria substantially alleviates the burden of variants of uncertain significance in ClinVar and LOVD databasesXiaoyu Yin, Marcy Richardson, Andreas Laner, et al.
Science (New York, N.Y.)|November 8, 2008
GENETICS. The Human Variome ProjectRichard G H Cotton, Arleen D Auerbach, Myles Axton, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 11, 2010
Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the colon cancer family registryMichael D Walsh, Daniel D Buchanan, Margaret C Cummings, et al.
American Journal of Human Genetics|November 28, 2002
The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish populationW D Foulkes, I Thiffault, S B Gruber, et al.
Journal of Crohn'S & Colitis|April 10, 2015
Effect of intestinal resection on quality of life in Crohn's diseaseEmily K Wright, Michael A Kamm, Peter De Cruz, et al.
Pageof 60