William Hotchkis Richmond Waters

Bằng Brown, David J
Được phát hành 2004

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

Bằng Brown, David J., Proulx, Michael J.
Được phát hành 2013

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

Bằng Haigh, Alastair, Brown, David J., Meijer, Peter, Proulx, Michael J.
Được phát hành 2013

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

Bằng Brown, David J., Simpson, Andrew J. R., Proulx, Michael J.
Xuất bản năm Front Psychol (2015)

Endoscopic Assisted Removal of a Massive Pediatric Floor of Mouth Dermoid

Bằng Kovatch, Kevin J, Baerg, Timothy, Ha, Jennifer F, Brown, David J
Xuất bản năm Ear Nose Throat J (2019)

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

Bằng McDermott, John C. B., Brown, David J., Britton, George, Goodwin, Trevor W.
Được phát hành 1974

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

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

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

Bằng 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.
Được phát hành 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...

Bằng 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.
Được phát hành 2002

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

Bằng 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.
Xuất bản năm Hum Mol Genet (2001)