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
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 1 |
2024 | 1 |
Search Results
2 results
Results by year
Filters applied: . Clear all
Page 1
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss.
Am J Med Genet A. 2024 Jun;194(6):e63563. doi: 10.1002/ajmg.a.63563. Epub 2024 Feb 14.
Am J Med Genet A. 2024.
PMID: 38352997
Identification of Main Genetic Causes Responsible for Non-Syndromic Hearing Loss in a Peruvian Population.
Figueroa-Ildefonso E, Bademci G, Rajabli F, Cornejo-Olivas M, Villanueva RDC, Badillo-Carrillo R, Inca-Martinez M, Neyra KM, Sineni C, Tekin M.
Figueroa-Ildefonso E, et al.
Genes (Basel). 2019 Jul 31;10(8):581. doi: 10.3390/genes10080581.
Genes (Basel). 2019.
PMID: 31370293
Free PMC article.
Item in Clipboard
Cite
Cite