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Journal of Inherited Metabolic Disease|January 1, 1980
D-2-hydroxyglutaric aciduria: case report and biochemical studiesR A Chalmers, A M Lawson, R W Watts, et al.
Lancet (London, England)|March 16, 1996
Polymorphism in serotonin transporter gene associated with susceptibility to major depressionA D Ogilvie, S Battersby, V J Bubb, et al.
Archives of Disease in Childhood|June 1, 1980
PseudohypoaldosteronismM J Dillon, J V Leonard, J M Buckler, et al.
Neuroreport|August 18, 1997
Allelic variation in the serotonin 5-HT2C receptor gene and migraineP W Burnet, P J Harrison, G M Goodwin, et al.
Evaluation and Program Planning|November 8, 2011
A community prevention model to prevent children from inhaling and ingesting harmful legal productsK W Johnson, J W Grube, K A Ogilvie, et al.
American Journal of Human Genetics|February 1, 1990
Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2B Sykes, D Ogilvie, P Wordsworth, et al.
Journal of Medical Genetics|April 1, 1991
Genetic analysis in cystic fibrosis using the amplification refractory mutation system (ARMS): the J3.11 MspI polymorphismC R Newton, C Summers, L E Heptinstall, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|February 3, 2005
The subjective and cognitive effects of acute phenylalanine and tyrosine depletion in patients recovered from depressionJonathan P Roiser, Andrew McLean, Alan D Ogilvie, et al.
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