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Biological Psychiatry
|
February 10, 1999
Whole blood serotonin and plasma beta-endorphin in autistic probands and their first-degree relatives
M Leboyer, A Philippe, M Bouvard, et al.
The Science of the Total Environment
|
January 27, 2020
Projecting life-cycle environmental impacts of corn production in the U.S. Midwest under future climate scenarios using a machine learning approach
Eun Kyung Lee, Wang-Jian Zhang, Xuesong Zhang, et al.
American Journal of Human Genetics
|
July 31, 1998
A high rate (20%-30%) of parental consanguinity in cytochrome-oxidase deficiency
J C von Kleist-Retzow, V Cormier-Daire, P de Lonlay, et al.
Psychiatry Research
|
February 1, 1992
Clinical subtypes and age at onset in schizophrenic siblings
M Leboyer, M J Filteau, M Jay, et al.
American Journal of Human Genetics
|
November 22, 2000
A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16
N Sylvius, F Tesson, C Gayet, et al.
Brain : a Journal of Neurology
|
February 1, 1996
Juvenile limb-girdle muscular dystrophy. Clinical, histopathological and genetic data from a small community living in the Reunion Island
M Fardeau, D Hillaire, C Mignard, et al.
Environmental Science. Processes & Impacts
|
January 10, 2015
River transport of mercury from artisanal and small-scale gold mining and risks for dietary mercury exposure in Madre de Dios, Peru
Sarah E Diringer, Beth J Feingold, Ernesto J Ortiz, et al.
Journal of Medical Genetics
|
October 4, 2002
Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience
P Charron, D Héron, M Gargiulo, et al.
Emerging Infectious Diseases
|
October 25, 2012
Livestock density as risk factor for livestock-associated methicillin-resistant Staphylococcus aureus, the Netherlands
Beth J Feingold, Ellen K Silbergeld, Frank C Curriero, et al.
Brain : a Journal of Neurology
|
November 11, 2003
Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/C
M Tazir, H Azzedine, S Assami, et al.
Page
of 31
Search research articles
Search
Showing results (261-270 of 307) with videos related to
Sort By:
Page
of 31
Biological Psychiatry
|
February 10, 1999
Whole blood serotonin and plasma beta-endorphin in autistic probands and their first-degree relatives
M Leboyer, A Philippe, M Bouvard, et al.
The Science of the Total Environment
|
January 27, 2020
Projecting life-cycle environmental impacts of corn production in the U.S. Midwest under future climate scenarios using a machine learning approach
Eun Kyung Lee, Wang-Jian Zhang, Xuesong Zhang, et al.
American Journal of Human Genetics
|
July 31, 1998
A high rate (20%-30%) of parental consanguinity in cytochrome-oxidase deficiency
J C von Kleist-Retzow, V Cormier-Daire, P de Lonlay, et al.
Psychiatry Research
|
February 1, 1992
Clinical subtypes and age at onset in schizophrenic siblings
M Leboyer, M J Filteau, M Jay, et al.
American Journal of Human Genetics
|
November 22, 2000
A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16
N Sylvius, F Tesson, C Gayet, et al.
Brain : a Journal of Neurology
|
February 1, 1996
Juvenile limb-girdle muscular dystrophy. Clinical, histopathological and genetic data from a small community living in the Reunion Island
M Fardeau, D Hillaire, C Mignard, et al.
Environmental Science. Processes & Impacts
|
January 10, 2015
River transport of mercury from artisanal and small-scale gold mining and risks for dietary mercury exposure in Madre de Dios, Peru
Sarah E Diringer, Beth J Feingold, Ernesto J Ortiz, et al.
Journal of Medical Genetics
|
October 4, 2002
Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience
P Charron, D Héron, M Gargiulo, et al.
Emerging Infectious Diseases
|
October 25, 2012
Livestock density as risk factor for livestock-associated methicillin-resistant Staphylococcus aureus, the Netherlands
Beth J Feingold, Ellen K Silbergeld, Frank C Curriero, et al.
Brain : a Journal of Neurology
|
November 11, 2003
Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/C
M Tazir, H Azzedine, S Assami, et al.
Page
of 31