William Hotchkis Richmond Waters

по Brown, David J
Опубликовано 2004

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

по Brown, David J., Proulx, Michael J.
Опубликовано 2013

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

по Haigh, Alastair, Brown, David J., Meijer, Peter, Proulx, Michael J.
Опубликовано 2013

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

по Brown, David J., Simpson, Andrew J. R., Proulx, Michael J.
Опубликовано в: Front Psychol (2015)

Endoscopic Assisted Removal of a Massive Pediatric Floor of Mouth Dermoid

по Kovatch, Kevin J, Baerg, Timothy, Ha, Jennifer F, Brown, David J
Опубликовано в: Ear Nose Throat J (2019)

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

по McDermott, John C. B., Brown, David J., Britton, George, Goodwin, Trevor W.
Опубликовано 1974

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

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

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

по 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.
Опубликовано 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...

по 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.
Опубликовано 2002

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

по 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.
Опубликовано в: Hum Mol Genet (2001)