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P Gustavsson

Showing results (91-100 of 110) with videos related to

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American Journal of Industrial Medicine|January 1, 1992
Lung cancer risk among workers exposed to man-made mineral fibers (MMMF) in the Swedish prefabricated house industryP Gustavsson, N Plato, O Axelson, et al.
Psychiatry Research|July 24, 1998
Polymorphisms in the dopamine, serotonin, and norepinephrine transporter genes and their relationships to monoamine metabolite concentrations in CSF of healthy volunteersE G Jönsson, M M Nöthen, J P Gustavsson, et al.
Clinical Genetics|May 3, 2006
Hemizygosity for chromosome 2q14.2-q22.1 spanning the GLI2 and PROC genes associated with growth hormone deficiency, polydactyly, deep vein thrombosis and urogenital abnormalitiesP Gustavsson, J Schoumans, J Staaf, et al.
European Journal of Human Genetics : EJHG|August 10, 1999
Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxiaD Tentler, P Gustavsson, J Leisti, et al.
The American Journal of Psychiatry|May 1, 1997
Lack of evidence for allelic association between personality traits and the dopamine D4 receptor gene polymorphismsE G Jönsson, M M Nöthen, J P Gustavsson, et al.
European Archives of Psychiatry and Clinical Neuroscience|January 1, 1997
Tryptophan hydroxylase and catechol-O-methyltransferase gene polymorphisms: relationships to monoamine metabolite concentrations in CSF of healthy volunteersE G Jönsson, D Goldman, G Spurlock, et al.
Psychological Medicine|September 2, 1998
Lack of association between dopamine D4 receptor gene and personality traitsE G Jönsson, M M Nöthen, J P Gustavsson, et al.
Genomics|August 7, 1998
Human calcium-activated potassium channel gene KCNN4 maps to chromosome 19q13.2 in the region deleted in diamond-blackfan anemiaS Ghanshani, M Coleman, P Gustavsson, et al.
The Journal of Clinical Endocrinology and Metabolism|June 8, 2000
Familial hypercalcemia and hypercalciuria caused by a novel mutation in the cytoplasmic tail of the calcium receptorT Carling, E Szabo, M Bai, et al.
American Journal of Medical Genetics|July 14, 1999
No association between serotonin transporter gene polymorphisms and personality traitsJ P Gustavsson, M M Nöthen, E G Jönsson, et al.
Pageof 11

Showing results (91-100 of 110) with videos related to

Sort By:
Pageof 11
American Journal of Industrial Medicine|January 1, 1992
Lung cancer risk among workers exposed to man-made mineral fibers (MMMF) in the Swedish prefabricated house industryP Gustavsson, N Plato, O Axelson, et al.
Psychiatry Research|July 24, 1998
Polymorphisms in the dopamine, serotonin, and norepinephrine transporter genes and their relationships to monoamine metabolite concentrations in CSF of healthy volunteersE G Jönsson, M M Nöthen, J P Gustavsson, et al.
Clinical Genetics|May 3, 2006
Hemizygosity for chromosome 2q14.2-q22.1 spanning the GLI2 and PROC genes associated with growth hormone deficiency, polydactyly, deep vein thrombosis and urogenital abnormalitiesP Gustavsson, J Schoumans, J Staaf, et al.
European Journal of Human Genetics : EJHG|August 10, 1999
Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxiaD Tentler, P Gustavsson, J Leisti, et al.
The American Journal of Psychiatry|May 1, 1997
Lack of evidence for allelic association between personality traits and the dopamine D4 receptor gene polymorphismsE G Jönsson, M M Nöthen, J P Gustavsson, et al.
European Archives of Psychiatry and Clinical Neuroscience|January 1, 1997
Tryptophan hydroxylase and catechol-O-methyltransferase gene polymorphisms: relationships to monoamine metabolite concentrations in CSF of healthy volunteersE G Jönsson, D Goldman, G Spurlock, et al.
Psychological Medicine|September 2, 1998
Lack of association between dopamine D4 receptor gene and personality traitsE G Jönsson, M M Nöthen, J P Gustavsson, et al.
Genomics|August 7, 1998
Human calcium-activated potassium channel gene KCNN4 maps to chromosome 19q13.2 in the region deleted in diamond-blackfan anemiaS Ghanshani, M Coleman, P Gustavsson, et al.
The Journal of Clinical Endocrinology and Metabolism|June 8, 2000
Familial hypercalcemia and hypercalciuria caused by a novel mutation in the cytoplasmic tail of the calcium receptorT Carling, E Szabo, M Bai, et al.
American Journal of Medical Genetics|July 14, 1999
No association between serotonin transporter gene polymorphisms and personality traitsJ P Gustavsson, M M Nöthen, E G Jönsson, et al.
Pageof 11