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American Journal of Human Genetics
|
November 1, 1996
Glutaric aciduria type I in the Arab and Jewish communities in Israel
Y Anikster, A Shaag, A Joseph, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Zellweger-like phenotype in two siblings: a defect in peroxisomal beta-oxidation with elevated very long-chain fatty acids but normal bile acids
H Mandel, M Berant, A Aizin, et al.
Journal of Inherited Metabolic Disease
|
March 28, 2002
Prolidase deficiency diagnosed by 1H NMR spectroscopy of urine
S H Moolenaar, U F Engelke, N G Abeling, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
January 1, 1995
Infantile Refsum disease: neonatal cholestatic jaundice presentation of a peroxisomal disorder
H Goez, D Meiron, J Horowitz, et al.
Professional Psychology, Research and Practice
|
February 10, 2016
Reply to comment on "Serving Transgender Youth: Challenges, Dilemmas, and Clinical Examples" by Tishelman et al. (2015)
Amy C Tishelman, Randi Kaufman, Laura Edwards-Leeper, et al.
Journal of Occupational and Environmental Medicine
|
July 3, 1999
Workplace influenza immunization update
J Burris, G W Olsen, M M Burlew, et al.
The Journal of Pediatrics
|
May 23, 2007
Chronic lung disease and cystic fibrosis phenotype in prolidase deficiency: a newly recognized association
A S Luder, H Mandel, M Khayat, et al.
Annals of Work Exposures and Health
|
November 16, 2020
A Bayesian Approach for Determining the Relationship Between Various Elongate Mineral Particles (EMPs) Definitions
Yuan Shao, Richard F MacLehose, Lifeng Lin, et al.
Annals of Epidemiology
|
September 19, 2015
Cancer incidence among Minnesota taconite mining industry workers
Elizabeth M Allen, Bruce H Alexander, Richard F MacLehose, et al.
Prenatal Diagnosis
|
August 19, 1999
Prenatal diagnosis of non-ketotic hyperglycinaemia: enzymatic diagnosis in 28 families and DNA diagnosis detecting prevalent Finnish and Israeli-Arab mutations
S Kure, M O Rolland, J Leisti, et al.
Page
of 19
Search research articles
Search
Showing results (111-120 of 188) with videos related to
Sort By:
Page
of 19
American Journal of Human Genetics
|
November 1, 1996
Glutaric aciduria type I in the Arab and Jewish communities in Israel
Y Anikster, A Shaag, A Joseph, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Zellweger-like phenotype in two siblings: a defect in peroxisomal beta-oxidation with elevated very long-chain fatty acids but normal bile acids
H Mandel, M Berant, A Aizin, et al.
Journal of Inherited Metabolic Disease
|
March 28, 2002
Prolidase deficiency diagnosed by 1H NMR spectroscopy of urine
S H Moolenaar, U F Engelke, N G Abeling, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
January 1, 1995
Infantile Refsum disease: neonatal cholestatic jaundice presentation of a peroxisomal disorder
H Goez, D Meiron, J Horowitz, et al.
Professional Psychology, Research and Practice
|
February 10, 2016
Reply to comment on "Serving Transgender Youth: Challenges, Dilemmas, and Clinical Examples" by Tishelman et al. (2015)
Amy C Tishelman, Randi Kaufman, Laura Edwards-Leeper, et al.
Journal of Occupational and Environmental Medicine
|
July 3, 1999
Workplace influenza immunization update
J Burris, G W Olsen, M M Burlew, et al.
The Journal of Pediatrics
|
May 23, 2007
Chronic lung disease and cystic fibrosis phenotype in prolidase deficiency: a newly recognized association
A S Luder, H Mandel, M Khayat, et al.
Annals of Work Exposures and Health
|
November 16, 2020
A Bayesian Approach for Determining the Relationship Between Various Elongate Mineral Particles (EMPs) Definitions
Yuan Shao, Richard F MacLehose, Lifeng Lin, et al.
Annals of Epidemiology
|
September 19, 2015
Cancer incidence among Minnesota taconite mining industry workers
Elizabeth M Allen, Bruce H Alexander, Richard F MacLehose, et al.
Prenatal Diagnosis
|
August 19, 1999
Prenatal diagnosis of non-ketotic hyperglycinaemia: enzymatic diagnosis in 28 families and DNA diagnosis detecting prevalent Finnish and Israeli-Arab mutations
S Kure, M O Rolland, J Leisti, et al.
Page
of 19