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Human Molecular Genetics|October 1, 1994
Characterization of a cystathionine beta-synthase allele with three mutations in cis in a patient with B6 nonresponsive homocystinuriaM Marble, M T Geraghty, R de Franchis, et al.Pediatrics|August 5, 2015
Novel WDR45 Mutation and Pathognomonic BPAN Imaging in a Young Female With Mild Cognitive DelayMichelle Long, Nishard Abdeen, Michael T Geraghty, et al.Plos Biology|December 10, 2021
Noise increases the correspondence between artificial and human visionJessica A F ThompsonJournal of Adolescence|September 1, 1985
The representation of authority: an adolescent viewpointC Murray, F ThompsonJournal of Neurophysiology|October 13, 2021
Forms of explanation and understanding for neuroscience and artificial intelligenceJessica A F ThompsonJournal of Inherited Metabolic Disease|May 9, 2000
Three cases of intravenous sodium benzoate and sodium phenylacetate toxicity occurring in the treatment of acute hyperammonaemiaV Praphanphoj, S A Boyadjiev, L J Waber, et al.Genomics|May 1, 1991
Ornithine aminotransferase-related sequences map to two nonadjacent intervals on the human X chromosome short armR G Lafreniere, M T Geraghty, D Valle, et al.Journal of Medical Genetics|April 1, 1988
Linkage analysis of X linked retinitis pigmentosa in the Irish populationG J Farrar, M T Geraghty, J M Moloney, et al.The Journal of Pediatrics|September 10, 2002
Joint hypermobility is more common in children with chronic fatigue syndrome than in healthy controlsDiana F Barron, Bernard A Cohen, Michael T Geraghty, et al.Molecular Genetics and Metabolism|April 5, 2001
Identification of the alpha-aminoadipic semialdehyde dehydrogenase-phosphopantetheinyl transferase gene, the human ortholog of the yeast LYS5 geneV Praphanphoj, K A Sacksteder, S J Gould, et al.Pageof 205