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
2 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Publication Date timeline is not available.
Page 1
Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia.
Am J Hum Genet. 1999 Dec;65(6):1803-6. doi: 10.1086/302658.
Am J Hum Genet. 1999.
PMID: 10577941
Free PMC article.
No abstract available.
GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf.
Tekin M, Xia XJ, Erdenetungalag R, Cengiz FB, White TW, Radnaabazar J, Dangaasuren B, Tastan H, Nance WE, Pandya A.
Tekin M, et al. Among authors: dangaasuren b.
Ann Hum Genet. 2010 Mar;74(2):155-64. doi: 10.1111/j.1469-1809.2010.00564.x. Epub 2010 Jan 27.
Ann Hum Genet. 2010.
PMID: 20201936
Free PMC article.
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.