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

N M Lindor

Showing results (31-40 of 59) with videos related to

Pageof 6
Sort By:
American Journal of Medical Genetics|September 1, 1992
Xp22.3 microdeletion syndrome with microphthalmia, sclerocornea, linear skin defects, and congenital heart defectsN M Lindor, V V Michels, D A Hoppe, et al.
Cancer Genetics and Cytogenetics|July 2, 1998
Search for chromosome instability in lymphocytes with germ-line mutations in DNA mismatch repair genesN M Lindor, S M Jalal, T J VanDeWalker, et al.
Gastroenterology|October 31, 1998
Familial predisposition for colorectal cancer in chronic ulcerative colitis: a case-control studyK W Nuako, D A Ahlquist, D W Mahoney, et al.
American Journal of Medical Genetics|May 26, 1999
Guidelines for buccal smear collection in breast-fed infantsD Babovic-Vuksanovic, V V Michels, M E Law, et al.
Human Heredity|March 17, 1999
Hereditary desmoid disease in a family with a germline Alu I repeat mutation of the APC geneK C Halling, C R Lazzaro, R Honchel, et al.
American Journal of Medical Genetics|June 1, 1993
Absence of chromosome fragility at 19q13.3 in patients with myotonic dystrophyS M Jalal, N M Lindor, V V Michels, et al.
Cancer|July 10, 2001
Germline E-cadherin gene mutations: is prophylactic total gastrectomy indicated?Y S Chun, N M Lindor, T C Smyrk, et al.
Breast Cancer Research and Treatment|January 14, 2000
p73 mutations are not detected in sporadic and hereditary breast cancerD I Schwartz, N M Lindor, C Walsh-Vockley, et al.
British Journal of Cancer|March 21, 2013
KRAS-mutation status in relation to colorectal cancer survival: the joint impact of correlated tumour markersA I Phipps, D D Buchanan, K W Makar, et al.
Journal of Medical Genetics|February 10, 2006
Connective tissue dysplasia in five new patients with NF1 microdeletions: further expansion of phenotype and review of the literatureK A Mensink, R P Ketterling, H C Flynn, et al.
Pageof 6

Showing results (31-40 of 59) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics|September 1, 1992
Xp22.3 microdeletion syndrome with microphthalmia, sclerocornea, linear skin defects, and congenital heart defectsN M Lindor, V V Michels, D A Hoppe, et al.
Cancer Genetics and Cytogenetics|July 2, 1998
Search for chromosome instability in lymphocytes with germ-line mutations in DNA mismatch repair genesN M Lindor, S M Jalal, T J VanDeWalker, et al.
Gastroenterology|October 31, 1998
Familial predisposition for colorectal cancer in chronic ulcerative colitis: a case-control studyK W Nuako, D A Ahlquist, D W Mahoney, et al.
American Journal of Medical Genetics|May 26, 1999
Guidelines for buccal smear collection in breast-fed infantsD Babovic-Vuksanovic, V V Michels, M E Law, et al.
Human Heredity|March 17, 1999
Hereditary desmoid disease in a family with a germline Alu I repeat mutation of the APC geneK C Halling, C R Lazzaro, R Honchel, et al.
American Journal of Medical Genetics|June 1, 1993
Absence of chromosome fragility at 19q13.3 in patients with myotonic dystrophyS M Jalal, N M Lindor, V V Michels, et al.
Cancer|July 10, 2001
Germline E-cadherin gene mutations: is prophylactic total gastrectomy indicated?Y S Chun, N M Lindor, T C Smyrk, et al.
Breast Cancer Research and Treatment|January 14, 2000
p73 mutations are not detected in sporadic and hereditary breast cancerD I Schwartz, N M Lindor, C Walsh-Vockley, et al.
British Journal of Cancer|March 21, 2013
KRAS-mutation status in relation to colorectal cancer survival: the joint impact of correlated tumour markersA I Phipps, D D Buchanan, K W Makar, et al.
Journal of Medical Genetics|February 10, 2006
Connective tissue dysplasia in five new patients with NF1 microdeletions: further expansion of phenotype and review of the literatureK A Mensink, R P Ketterling, H C Flynn, et al.
Pageof 6