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

Carol Cremin

Showing results (21-30 of 24) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 24 results.
Clinical and Translational Gastroenterology|August 16, 2021
Integrating Tumor Sequencing Into Clinical Practice for Patients With Mismatch Repair-Deficient Lynch Syndrome Spectrum CancersKatherine Dixon, Mary-Jill Asrat, Angela C Bedard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 7, 2020
Improved structural variant interpretation for hereditary cancer susceptibility using long-read sequencingMy Linh Thibodeau, Kieran O'Neill, Katherine Dixon, et al.
Cold Spring Harbor Molecular Case Studies|March 6, 2019
Base excision repair deficiency signatures implicate germline and somatic <i>MUTYH</i> aberrations in pancreatic ductal adenocarcinoma and breast cancer oncogenesisMy Linh Thibodeau, Eric Y Zhao, Caralyn Reisle, et al.
Journal of Medical Genetics|March 15, 2011
Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinomaBetty Gardie, Audrey Remenieras, Darouna Kattygnarath, et al.
Pageof 3

Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
Clinical and Translational Gastroenterology|August 16, 2021
Integrating Tumor Sequencing Into Clinical Practice for Patients With Mismatch Repair-Deficient Lynch Syndrome Spectrum CancersKatherine Dixon, Mary-Jill Asrat, Angela C Bedard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 7, 2020
Improved structural variant interpretation for hereditary cancer susceptibility using long-read sequencingMy Linh Thibodeau, Kieran O'Neill, Katherine Dixon, et al.
Cold Spring Harbor Molecular Case Studies|March 6, 2019
Base excision repair deficiency signatures implicate germline and somatic <i>MUTYH</i> aberrations in pancreatic ductal adenocarcinoma and breast cancer oncogenesisMy Linh Thibodeau, Eric Y Zhao, Caralyn Reisle, et al.
Journal of Medical Genetics|March 15, 2011
Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinomaBetty Gardie, Audrey Remenieras, Darouna Kattygnarath, et al.
Pageof 3