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

Philip H Gordon

Showing results (21-30 of 25) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 25 results.
Familial Cancer|March 11, 2006
The value of multi-modal gene screening in HNPCC in Quebec: three mutations in mismatch repair genes that would have not been correctly identified by genomic DNA sequencing aloneSusan McVety, Lili Li, Isabelle Thiffault, et al.
Nutrition Journal|November 12, 2013
Dynamics of vitamin D in patients with mild or inactive inflammatory bowel disease and their familiesAvigyle Grunbaum, Christina Holcroft, Debra Heilpern, et al.
Human Mutation|March 17, 2006
Distinct patterns of germ-line deletions in MLH1 and MSH2: the implication of Alu repetitive element in the genetic etiology of Lynch syndrome (HNPCC)Lili Li, Susan McVety, Rami Younan, et al.
Journal of Gastrointestinal Surgery : Official Journal of the Society for Surgery of the Alimentary Tract|April 11, 2015
Normalization of CEA Levels Post-Neoadjuvant Therapy is a Strong Predictor of Pathologic Complete Response in Rectal CancerAriella Kleiman, Ahmed Al-Khamis, Ali Farsi, et al.
Human Mutation|May 22, 2009
High frequency of exon deletions and putative founder effects in French Canadian Lynch syndrome familiesGeorge Chong, Jonathan Jarry, Victoria Marcus, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Familial Cancer|March 11, 2006
The value of multi-modal gene screening in HNPCC in Quebec: three mutations in mismatch repair genes that would have not been correctly identified by genomic DNA sequencing aloneSusan McVety, Lili Li, Isabelle Thiffault, et al.
Nutrition Journal|November 12, 2013
Dynamics of vitamin D in patients with mild or inactive inflammatory bowel disease and their familiesAvigyle Grunbaum, Christina Holcroft, Debra Heilpern, et al.
Human Mutation|March 17, 2006
Distinct patterns of germ-line deletions in MLH1 and MSH2: the implication of Alu repetitive element in the genetic etiology of Lynch syndrome (HNPCC)Lili Li, Susan McVety, Rami Younan, et al.
Journal of Gastrointestinal Surgery : Official Journal of the Society for Surgery of the Alimentary Tract|April 11, 2015
Normalization of CEA Levels Post-Neoadjuvant Therapy is a Strong Predictor of Pathologic Complete Response in Rectal CancerAriella Kleiman, Ahmed Al-Khamis, Ali Farsi, et al.
Human Mutation|May 22, 2009
High frequency of exon deletions and putative founder effects in French Canadian Lynch syndrome familiesGeorge Chong, Jonathan Jarry, Victoria Marcus, et al.
Pageof 3