Search Page
Save citations to file
Email citations
On or after July 28, sending email will require My NCBI login.
Learn more about this and other changes coming to the email feature.
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
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2000 | 1 |
2001 | 1 |
2003 | 1 |
2025 | 0 |
Search Results
3 results
Results by year
Filters applied: . Clear all
Page 1
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness.
J Med Genet. 2003 Apr;40(4):242-8. doi: 10.1136/jmg.40.4.242.
J Med Genet. 2003.
PMID: 12676893
Free PMC article.
Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness.
Liu XZ, Xia XJ, Adams J, Chen ZY, Welch KO, Tekin M, Ouyang XM, Kristiansen A, Pandya A, Balkany T, Arnos KS, Nance WE.
Liu XZ, et al.
Hum Mol Genet. 2001 Dec 1;10(25):2945-51. doi: 10.1093/hmg/10.25.2945.
Hum Mol Genet. 2001.
PMID: 11741837
Item in Clipboard
Relation between choice of partner and high frequency of connexin-26 deafness.
Nance WE, Liu XZ, Pandya A.
Nance WE, et al.
Lancet. 2000 Aug 5;356(9228):500-1. doi: 10.1016/S0140-6736(00)02565-4.
Lancet. 2000.
PMID: 10981905
Item in Clipboard
Cite
Cite
ARTICLE TYPE
ARTICLE LANGUAGE
AGE
Filters on the sidebar will be reset to the default list and any currently applied filters will be cleared.