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
USH2A gene variants cause Keratoconus and Usher syndrome phenotypes in Pakistani families.
BMC Ophthalmol. 2021 Apr 29;21(1):191. doi: 10.1186/s12886-021-01957-9.
BMC Ophthalmol. 2021.
PMID: 33926394
Free PMC article.
Novel mutations in PDE6A and CDHR1 cause retinitis pigmentosa in Pakistani families.
Dawood M, Lin S, Din TU, Shah IU, Khan N, Jan A, Marwan M, Sultan K, Nowshid M, Tahir R, Ahmed AN, Yasin M, Baple EL, Crosby AH, Saleha S.
Dawood M, et al. Among authors: nowshid m.
Int J Ophthalmol. 2021 Dec 18;14(12):1843-1851. doi: 10.18240/ijo.2021.12.06. eCollection 2021.
Int J Ophthalmol. 2021.
PMID: 34926197
Free PMC article.
Item in Clipboard
Maternal FMR1 alleles expansion in newborns during transmission: a prospective cohort study.
Shahid R, Yasin M, Rehman ZU, Jadoon H, Tahir H, Meraj N, Khan N, Zubair M, Zulfiqar I, Nowshid M, Azeem A, Jabeen M, Hameed A, Saleha S.
Shahid R, et al. Among authors: nowshid m.
Pediatr Res. 2023 Feb;93(3):720-724. doi: 10.1038/s41390-022-02128-2. Epub 2022 Jun 9.
Pediatr Res. 2023.
PMID: 35681093
Item in Clipboard
Cite
Cite