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Maternal FMR1 alleles expansion in newborns during transmission: a prospective cohort study.
Pediatr Res. 2023 Feb;93(3):720-724. doi: 10.1038/s41390-022-02128-2. Epub 2022 Jun 9.
Pediatr Res. 2023.
PMID: 35681093
USH2A gene variants cause Keratoconus and Usher syndrome phenotypes in Pakistani families.
Ahmed AN, Tahir R, Khan N, Ahmad M, Dawood M, Basit A, Yasin M, Nowshid M, Marwan M, Sultan K, Saleha S.
Ahmed AN, et al. Among authors: nowshid m.
BMC Ophthalmol. 2021 Apr 29;21(1):191. doi: 10.1186/s12886-021-01957-9.
BMC Ophthalmol. 2021.
PMID: 33926394
Free PMC article.
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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.
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