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

J T Coulombe

Showing results (1-10 of 6) with videos related to

Pageof 1
Sort By:
Pediatrics|October 1, 1984
Massachusetts Metabolic Disorders Screening Program: III. SarcosinemiaH L Levy, J T Coulombe, R Benjamin
Pediatrics|January 1, 1981
Massachusetts Metabolic Disorders Screening Program. II. Methylmalonic aciduriaJ T Coulombe, V E Shih, H L Levy
The New England Journal of Medicine|December 2, 1976
Methylmalonic aciduria in the newbornV E Shih, J T Coulombe, M Maties, et al.
Clinical Genetics|September 1, 1984
Occurrences of methylmalonic aciduria and Hartnup disorder in the same familyV E Shih, J T Coulombe, S K Wadman, et al.
Pediatric Research|March 1, 1984
Congenital expression of prolidase defect in prolidase deficiencyE R Naughten, S P Proctor, H L Levy, et al.
Journal of Inherited Metabolic Disease|January 1, 1983
Histidinaemia. Part III: Impact; a prospective studyJ T Coulombe, B L Kammerer, H L Levy, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Pediatrics|October 1, 1984
Massachusetts Metabolic Disorders Screening Program: III. SarcosinemiaH L Levy, J T Coulombe, R Benjamin
Pediatrics|January 1, 1981
Massachusetts Metabolic Disorders Screening Program. II. Methylmalonic aciduriaJ T Coulombe, V E Shih, H L Levy
The New England Journal of Medicine|December 2, 1976
Methylmalonic aciduria in the newbornV E Shih, J T Coulombe, M Maties, et al.
Clinical Genetics|September 1, 1984
Occurrences of methylmalonic aciduria and Hartnup disorder in the same familyV E Shih, J T Coulombe, S K Wadman, et al.
Pediatric Research|March 1, 1984
Congenital expression of prolidase defect in prolidase deficiencyE R Naughten, S P Proctor, H L Levy, et al.
Journal of Inherited Metabolic Disease|January 1, 1983
Histidinaemia. Part III: Impact; a prospective studyJ T Coulombe, B L Kammerer, H L Levy, et al.
Pageof 1