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

D Markie

Showing results (21-30 of 28) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 28 results.
Human Molecular Genetics|November 13, 1998
Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of casesR Houlston, S Bevan, A Williams, et al.
Nature|January 15, 1998
A serine/threonine kinase gene defective in Peutz-Jeghers syndromeA Hemminki, D Markie, I Tomlinson, et al.
Journal of Medical Genetics|February 25, 1998
Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3S Olschwang, D Markie, S Seal, et al.
Scientific Reports|May 11, 2017
An ovine hepatorenal fibrocystic model of a Meckel-like syndrome associated with dysmorphic primary cilia and TMEM67 mutationsC Stayner, C A Poole, S R McGlashan, et al.
Cancer Research|November 26, 1997
Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndromeD J Marsh, S Roth, K L Lunetta, et al.
Gut|April 15, 2000
Analysis of genetic and phenotypic heterogeneity in juvenile polyposisK Woodford-Richens, S Bevan, M Churchman, et al.
American Journal of Human Genetics|September 6, 2001
Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromesX P Zhou, K Woodford-Richens, R Lehtonen, et al.
Science (New York, N.Y.)|July 11, 1997
Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasisE D Carstea, J A Morris, K G Coleman, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Human Molecular Genetics|November 13, 1998
Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of casesR Houlston, S Bevan, A Williams, et al.
Nature|January 15, 1998
A serine/threonine kinase gene defective in Peutz-Jeghers syndromeA Hemminki, D Markie, I Tomlinson, et al.
Journal of Medical Genetics|February 25, 1998
Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3S Olschwang, D Markie, S Seal, et al.
Scientific Reports|May 11, 2017
An ovine hepatorenal fibrocystic model of a Meckel-like syndrome associated with dysmorphic primary cilia and TMEM67 mutationsC Stayner, C A Poole, S R McGlashan, et al.
Cancer Research|November 26, 1997
Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndromeD J Marsh, S Roth, K L Lunetta, et al.
Gut|April 15, 2000
Analysis of genetic and phenotypic heterogeneity in juvenile polyposisK Woodford-Richens, S Bevan, M Churchman, et al.
American Journal of Human Genetics|September 6, 2001
Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromesX P Zhou, K Woodford-Richens, R Lehtonen, et al.
Science (New York, N.Y.)|July 11, 1997
Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasisE D Carstea, J A Morris, K G Coleman, et al.
Pageof 3