William Hotchkis Richmond Waters

Tekijä Brown, David J
Julkaistu 2004

Increased Signal Complexity Improves the Breadth of Generalization in Auditory Perceptual Learning

Tekijä Brown, David J., Proulx, Michael J.
Julkaistu 2013

How well do you see what you hear? The acuity of visual-to-auditory sensory substitution

Tekijä Haigh, Alastair, Brown, David J., Meijer, Peter, Proulx, Michael J.
Julkaistu 2013

Auditory scene analysis and sonified visual images. Does consonance negatively impact on object formation when using complex sonified stimuli?

Tekijä Brown, David J., Simpson, Andrew J. R., Proulx, Michael J.
Julkaisussa Front Psychol (2015)

Endoscopic Assisted Removal of a Massive Pediatric Floor of Mouth Dermoid

Tekijä Kovatch, Kevin J, Baerg, Timothy, Ha, Jennifer F, Brown, David J
Julkaisussa Ear Nose Throat J (2019)

Alternative pathways of zeaxanthin biosynthesis in a Flavobacterium species. Experiments with nicotine as inhibitor

Tekijä McDermott, John C. B., Brown, David J., Britton, George, Goodwin, Trevor W.
Julkaistu 1974

Other ways of seeing: From behavior to neural mechanisms in the online “visual” control of action with sensory substitution

Tekijä Proulx, Michael J., Gwinnutt, James, Dell’Erba, Sara, Levy-Tzedek, Shelly, de Sousa, Alexandra A., Brown, David J.
Julkaisussa Restor Neurol Neurosci (2015)

Mathematical Model Developed for Environmental Samples: Prediction of GC/MS Dioxin TEQ from XDS-CALUX Bioassay Data

Tekijä Brown, David J., Orelien, Jean, Gordon, John D., Chu, Andrew C., Chu, Michael D., Nakamura, Masafumi, Handa, Hiroshi, Kayama, Fujio, Denison, Michael S., Clark, George C.
Julkaistu 2007

Autosomal Dominant Stapes Ankylosis with Broad Thumbs and Toes, Hyperopia, and Skeletal Anomalies Is Caused by Heterozygous Nonsense and Frameshift Mutations in NOG, the Gene Encod...

Tekijä Brown, David J., Kim, Theresa B., Petty, Elizabeth M., Downs, Catherine A., Martin, Donna M., Strouse, Peter J., Moroi, Sayoko E., Milunsky, Jeff M., Lesperance, Marci M.
Julkaistu 2002

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss

Tekijä Bespalova, Irina N., Van Camp, Guy, Bom, Steven J.H., Brown, David J., Cryns, Kim, DeWan, Andrew T., Erson, Ayse E., Flothmann, Kris, Kunst, Henricus P.M., Kurnool, Purnima, Sivakumaran, Theru A., Cremers, Cor W.R.J., Leal, Suzanne M., Burmeister, Margit, Lesperance, Marci M.
Julkaisussa Hum Mol Genet (2001)