Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
3 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness.
Am J Hum Genet. 2012 Feb 10;90(2):321-30. doi: 10.1016/j.ajhg.2011.12.007.
Am J Hum Genet. 2012.
PMID: 22325361
Free PMC article.
Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness.
Zeitz C, Jacobson SG, Hamel CP, Bujakowska K, Neuillé M, Orhan E, Zanlonghi X, Lancelot ME, Michiels C, Schwartz SB, Bocquet B; Congenital Stationary Night Blindness Consortium; Antonio A, Audier C, Letexier M, Saraiva JP, Luu TD, Sennlaub F, Nguyen H, Poch O, Dollfus H, Lecompte O, Kohl S, Sahel JA, Bhattacharya SS, Audo I.
Zeitz C, et al. Among authors: audier c.
Am J Hum Genet. 2013 Jan 10;92(1):67-75. doi: 10.1016/j.ajhg.2012.10.023. Epub 2012 Dec 13.
Am J Hum Genet. 2013.
PMID: 23246293
Free PMC article.
Item in Clipboard
Money for medication: a randomized controlled study on the effectiveness of financial incentives to improve medication adherence in patients with psychotic disorders.
Noordraven EL, Audier CH, Staring AB, Wierdsma AI, Blanken P, van der Hoorn BE, Roijen LH, Mulder CL.
Noordraven EL, et al. Among authors: audier ch.
BMC Psychiatry. 2014 Dec 2;14:343. doi: 10.1186/s12888-014-0343-3.
BMC Psychiatry. 2014.
PMID: 25438877
Free PMC article.
Clinical Trial.
Item in Clipboard
Cite
Cite