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 Mowat

Showing results (11-20 of 30) with videos related to

Pageof 3
Sort By:
Reproductive Biomedicine Online|April 14, 2010
Russell-Silver syndrome due to paternal H19/IGF2 hypomethylation in a patient conceived using intracytoplasmic sperm injectionM Chopra, D J Amor, L Sutton, et al.
Environmental Science & Technology|May 27, 2011
Influence of forest canopies on the deposition of methylmercury to boreal ecosystem watershedsLinnea D Mowat, Vincent L St Louis, Jennifer A Graydon, et al.
Clinical Genetics|December 3, 2013
Mutations of codon 2085 in the helicase domain of ATRX are recurrent and cause ATRX syndromeC Lacoste, B Leheup, I Agouti, et al.
Australasian Radiology|August 1, 1988
Audit as a basis for informed consent with cerebral angiographyP D Mowat, T M McGuire, L B Jellett, et al.
Canadian Family Physician Medecin De Famille Canadien|July 1, 1996
Delisting of drugs in Ontario. How attitudes and prescribing strategies of family physicians in the Kingston area changedM Godwin, J Chapman, D Mowat, et al.
The Journal of Pediatrics|March 4, 1999
Respiratory chain complex III [correction of complex] in deficiency with pruritus: a novel vitamin responsive clinical featureD Mowat, D M Kirby, K R Kamath, et al.
Clinical Genetics|November 15, 2006
Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanismR H Hämäläinen, D Mowat, M T Gabbett, et al.
Current Oncology (Toronto, Ont.)|June 23, 2016
Smoking behaviours of current cancer patients in CanadaJ Liu, J Chadder, S Fung, et al.
Australasian Radiology|November 17, 2006
Familial cerebral cavernous haemangioma diagnosed in an infant with a rapidly growing cerebral lesionB H K Ng, E Mulyadi, J K Pereira, et al.
American Journal of Medical Genetics. Part A|July 12, 2005
Pallister-Hall syndrome: unreported skeletal features of a GLI3 mutationT Roscioli, D Kennedy, J Cui, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Reproductive Biomedicine Online|April 14, 2010
Russell-Silver syndrome due to paternal H19/IGF2 hypomethylation in a patient conceived using intracytoplasmic sperm injectionM Chopra, D J Amor, L Sutton, et al.
Environmental Science & Technology|May 27, 2011
Influence of forest canopies on the deposition of methylmercury to boreal ecosystem watershedsLinnea D Mowat, Vincent L St Louis, Jennifer A Graydon, et al.
Clinical Genetics|December 3, 2013
Mutations of codon 2085 in the helicase domain of ATRX are recurrent and cause ATRX syndromeC Lacoste, B Leheup, I Agouti, et al.
Australasian Radiology|August 1, 1988
Audit as a basis for informed consent with cerebral angiographyP D Mowat, T M McGuire, L B Jellett, et al.
Canadian Family Physician Medecin De Famille Canadien|July 1, 1996
Delisting of drugs in Ontario. How attitudes and prescribing strategies of family physicians in the Kingston area changedM Godwin, J Chapman, D Mowat, et al.
The Journal of Pediatrics|March 4, 1999
Respiratory chain complex III [correction of complex] in deficiency with pruritus: a novel vitamin responsive clinical featureD Mowat, D M Kirby, K R Kamath, et al.
Clinical Genetics|November 15, 2006
Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanismR H Hämäläinen, D Mowat, M T Gabbett, et al.
Current Oncology (Toronto, Ont.)|June 23, 2016
Smoking behaviours of current cancer patients in CanadaJ Liu, J Chadder, S Fung, et al.
Australasian Radiology|November 17, 2006
Familial cerebral cavernous haemangioma diagnosed in an infant with a rapidly growing cerebral lesionB H K Ng, E Mulyadi, J K Pereira, et al.
American Journal of Medical Genetics. Part A|July 12, 2005
Pallister-Hall syndrome: unreported skeletal features of a GLI3 mutationT Roscioli, D Kennedy, J Cui, et al.
Pageof 3