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Page 1
Identification of candidate regions for a novel Usher syndrome type II locus.
Ben Rebeh I, Benzina Z, Dhouib H, Hadjamor I, Amyere M, Ayadi L, Turki K, Hammami B, Kmiha N, Kammoun H, Hakim B, Charfedine I, Vikkula M, Ghorbel A, Ayadi H, Masmoudi S. Ben Rebeh I, et al. Among authors: hammami b. Mol Vis. 2008 Sep 19;14:1719-26. Mol Vis. 2008. PMID: 18806881 Free PMC article.
A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60.
Ben Said M, Grati M, Ishimoto T, Zou B, Chakchouk I, Ma Q, Yao Q, Hammami B, Yan D, Mittal R, Nakamichi N, Ghorbel A, Neng L, Tekin M, Shi XR, Kato Y, Masmoudi S, Lu Z, Hmani M, Liu X. Ben Said M, et al. Among authors: hammami b. Hum Genet. 2016 May;135(5):513-524. doi: 10.1007/s00439-016-1657-7. Epub 2016 Mar 29. Hum Genet. 2016. PMID: 27023905 Free PMC article.
Organized Hematoma of the Maxillary Sinus: Report of Two Cases.
Chaabouni MA, Kallel S, Kharrat R, Kharrat I, Mellouli M, Hammami B, Charfeddine I. Chaabouni MA, et al. Among authors: hammami b. Iran J Otorhinolaryngol. 2021 May;33(116):177-181. doi: 10.22038/ijorl.2021.48295.2594. Iran J Otorhinolaryngol. 2021. PMID: 34222110 Free PMC article.
114 results