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Joint Commission Journal on Quality and Patient Safety
|
June 28, 2021
Prevalence and Characteristics of Interruptions and Distractions During Surgical Counts
Katherine A Bubric, Susan L Biesbroek, Jason C Laberge, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Prospective ascertainment of complete and partial serum biotinidase deficiency in the newborn
G Dunkel, C R Scriver, C L Clow, et al.
Diabetes Care
|
June 2, 2000
Impact of diabetes on crash risks of truck-permit holders and commercial drivers
C Laberge-Nadeau, G Dionne, J M Ekoé, et al.
Accident; Analysis and Prevention
|
October 1, 1993
Exposure for different license categories through a phone survey: validity and feasibility studies
P Joly, M F Joly, D Desjardins, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1980
Cord-blood tyrosine levels in the full-term phenylketonuric fetus and the "justification hypothesis"
C R Scriver, D E Cole, S A Houghton, et al.
Pediatric Pulmonology
|
December 9, 2008
Inter- and intra-rater reliability of neck circumference measurements in children
Robert C LaBerge, Jean Philippe Vaccani, Robert M Gow, et al.
International Journal of Epidemiology
|
October 3, 1998
Socioeconomic geographical links to human immunodeficiency virus seroprevalence among childbearing women in Montreal, 1989-1993
C Hankins, T Tran, L Hum, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
February 1, 1989
Myotonic dystrophy: linkage with apolipoprotein E and estimation of the gene carrier status with genetic markers
M C Thibault, J Mathieu, S Moorjani, et al.
American Journal of Human Genetics
|
August 1, 1990
Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I)
R M Tanguay, J P Valet, A Lescault, et al.
American Journal of Human Genetics
|
May 1, 1987
The Hartnup phenotype: Mendelian transport disorder, multifactorial disease
C R Scriver, B Mahon, H L Levy, et al.
Page
of 12
Search research articles
Search
Showing results (91-100 of 111) with videos related to
Sort By:
Page
of 12
Joint Commission Journal on Quality and Patient Safety
|
June 28, 2021
Prevalence and Characteristics of Interruptions and Distractions During Surgical Counts
Katherine A Bubric, Susan L Biesbroek, Jason C Laberge, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Prospective ascertainment of complete and partial serum biotinidase deficiency in the newborn
G Dunkel, C R Scriver, C L Clow, et al.
Diabetes Care
|
June 2, 2000
Impact of diabetes on crash risks of truck-permit holders and commercial drivers
C Laberge-Nadeau, G Dionne, J M Ekoé, et al.
Accident; Analysis and Prevention
|
October 1, 1993
Exposure for different license categories through a phone survey: validity and feasibility studies
P Joly, M F Joly, D Desjardins, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1980
Cord-blood tyrosine levels in the full-term phenylketonuric fetus and the "justification hypothesis"
C R Scriver, D E Cole, S A Houghton, et al.
Pediatric Pulmonology
|
December 9, 2008
Inter- and intra-rater reliability of neck circumference measurements in children
Robert C LaBerge, Jean Philippe Vaccani, Robert M Gow, et al.
International Journal of Epidemiology
|
October 3, 1998
Socioeconomic geographical links to human immunodeficiency virus seroprevalence among childbearing women in Montreal, 1989-1993
C Hankins, T Tran, L Hum, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
February 1, 1989
Myotonic dystrophy: linkage with apolipoprotein E and estimation of the gene carrier status with genetic markers
M C Thibault, J Mathieu, S Moorjani, et al.
American Journal of Human Genetics
|
August 1, 1990
Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I)
R M Tanguay, J P Valet, A Lescault, et al.
American Journal of Human Genetics
|
May 1, 1987
The Hartnup phenotype: Mendelian transport disorder, multifactorial disease
C R Scriver, B Mahon, H L Levy, et al.
Page
of 12