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Rare NF1 microdeletion syndrome in an Omani patient.
Al-Araimi M, Hamza N, Al Yahmadi A, Al Mazrooey H, Elsheikh A, Al Amri A, Al Harrasi S, Hausdorf L, Mula-Abed WA. Al-Araimi M, et al. Clin Case Rep. 2018 Oct 26;6(12):2424-2426. doi: 10.1002/ccr3.1881. eCollection 2018 Dec. Clin Case Rep. 2018. PMID: 30564341 Free PMC article.
A First-Case Report of Pycnodysostosis in an Omani Boy.
Al-Araimi M, Al-Hosni A, Maimani AA. Al-Araimi M, et al. J Pediatr Genet. 2020 Aug 4;11(1):42-46. doi: 10.1055/s-0040-1714364. eCollection 2022 Mar. J Pediatr Genet. 2020. PMID: 35186389 Free PMC article.
16 results