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An unusual familial Xp22.12 microduplication including EIF1AX: A novel candidate dosage-sensitive gene for premature ovarian insufficiency.
Sakka R, Abdelhedi F, Sellami H, Pichon B, Lajmi Y, Mnif M, Kebaili S, Derbel R, Kamoun H, Gdoura R, Delbaere A, Desir J, Abramowicz M, Vialard F, Dupont JM, Ammar-Keskes L. Sakka R, et al. Among authors: derbel r. Eur J Med Genet. 2022 Nov;65(11):104613. doi: 10.1016/j.ejmg.2022.104613. Epub 2022 Sep 14. Eur J Med Genet. 2022. PMID: 36113757
Development of a simple genotyping method based on indel mutations to rapidly screen SARS-CoV-2 circulating variants: Delta, Omicron BA.1 and BA.2.
Ayadi W, Taktak A, Gargouri S, Smaoui F, Chtourou A, Skouri-Gargouri H, Derbel R, Sassi AH, Gargouri A, Hammami A, Karray-Hakim H, Mokdad-Gargouri R, Fki-Berrajah L. Ayadi W, et al. Among authors: derbel r. J Virol Methods. 2022 Sep;307:114570. doi: 10.1016/j.jviromet.2022.114570. Epub 2022 Jun 18. J Virol Methods. 2022. PMID: 35724698 Free PMC article.
18 results