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Page 1
Association of COL1A1 and TGFB1 polymorphisms with otosclerosis in a Tunisian population.
Khalfallah A, Schrauwen I, Mnejja M, HadjKacem H, Dhouib L, Mosrati MA, Hakim B, Lahmar I, Charfeddine I, Driss N, Ayadi H, Ghorbel A, Van Camp G, Masmoudi S. Khalfallah A, et al. Among authors: ghorbel a. Ann Hum Genet. 2011 Sep;75(5):598-604. doi: 10.1111/j.1469-1809.2011.00665.x. Epub 2011 Jul 21. Ann Hum Genet. 2011. PMID: 21777208
A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family.
Ben Saïd M, Ayedi L, Mnejja M, Hakim B, Khalfallah A, Charfeddine I, Khifagi C, Turki K, Ayadi H, Benzina Z, Ghorbel A, Castillo ID, Masmoudi S, Aifa MH. Ben Saïd M, et al. Among authors: ghorbel a. Eur J Med Genet. 2011 Nov-Dec;54(6):e535-41. doi: 10.1016/j.ejmg.2011.06.008. Epub 2011 Jul 13. Eur J Med Genet. 2011. PMID: 21802533
NADf chip, a two-color microarray for simultaneous screening of multigene mutations associated with hearing impairment in North African Mediterranean countries.
Chakchouk I, Ben Said M, Jbeli F, Benmarzoug R, Loukil S, Smeti I, Chakroun A, Gibriel AA, Ghorbel A, Hadjkacem H, Masmoudi S. Chakchouk I, et al. Among authors: ghorbel a. J Mol Diagn. 2015 Mar;17(2):155-61. doi: 10.1016/j.jmoldx.2014.11.003. Epub 2015 Jan 2. J Mol Diagn. 2015. PMID: 25560255 Free article.
CDH23 Methylation Status and Presbycusis Risk in Elderly Women.
Bouzid A, Smeti I, Chakroun A, Loukil S, Gibriel AA, Grati M, Ghorbel A, Masmoudi S. Bouzid A, et al. Among authors: ghorbel a. Front Aging Neurosci. 2018 Aug 7;10:241. doi: 10.3389/fnagi.2018.00241. eCollection 2018. Front Aging Neurosci. 2018. PMID: 30131691 Free PMC article.
317 results