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Page 1
The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families.
Al-Kasbi G, Al-Murshedi F, Al-Kindi A, Al-Hashimi N, Al-Thihli K, Al-Saegh A, Al-Futaisi A, Al-Mamari W, Al-Asmi A, Bruwer Z, Al-Kharusi K, Al-Rashdi S, Zadjali F, Al-Yahyaee S, Al-Maawali A. Al-Kasbi G, et al. Among authors: al mamari w. Sci Rep. 2022 Nov 7;12(1):18862. doi: 10.1038/s41598-022-22036-z. Sci Rep. 2022. PMID: 36344539 Free PMC article.
Learning Disabilities: Opportunities and challenges in Oman.
Al-Mahrezi A, Al-Futaisi A, Al-Mamari W. Al-Mahrezi A, et al. Sultan Qaboos Univ Med J. 2016 May;16(2):e129-31. doi: 10.18295/squmj.2016.16.02.001. Epub 2016 May 15. Sultan Qaboos Univ Med J. 2016. PMID: 27226902 Free PMC article. No abstract available.
LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss.
Al-Amri AH, Al Saegh A, Al-Mamari W, El-Asrag ME, Al-Kindi MN, Al Khabouri M, Al Wardy N, Al Lamki K, Gabr A, Idris A, Inglehearn CF, Clapcote SJ, Ali M. Al-Amri AH, et al. Eur J Med Genet. 2019 Dec;62(12):103592. doi: 10.1016/j.ejmg.2018.11.026. Epub 2018 Nov 23. Eur J Med Genet. 2019. PMID: 30476627
Telemedicine in the Era of COVID-19 and Beyond: A new horizon.
Alsaffar H, Almamari W, Al Futaisi A. Alsaffar H, et al. Sultan Qaboos Univ Med J. 2020 Nov;20(4):e277-e279. doi: 10.18295/squmj.2020.20.04.001. Epub 2020 Dec 21. Sultan Qaboos Univ Med J. 2020. PMID: 33414930 Free PMC article. No abstract available.
24 results