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Genetic studies in the Nigerian population implicate an MSX1 mutation in complex oral facial clefting disorders.
Butali A, Mossey PA, Adeyemo WL, Jezewski PA, Onwuamah CK, Ogunlewe MO, Ugboko VI, Adejuyigbe O, Adigun AI, Abdur-Rahman LO, Onah II, Audu RA, Idigbe EO, Mansilla MA, Dragan EA, Petrin AL, Bullard SA, Uduezue AO, Akpata O, Osaguona AO, Olasoji HO, Ligali TO, Kejeh BM, Iseh KR, Olaitan PB, Adebola AR, Efunkoya E, Adesina OA, Oluwatosin OM, Murray JC; NigeriaCRAN Collaboration. Butali A, et al. Among authors: oluwatosin om. Cleft Palate Craniofac J. 2011 Nov;48(6):646-53. doi: 10.1597/10-133. Epub 2011 Jul 8. Cleft Palate Craniofac J. 2011. PMID: 21740177 Free PMC article.
Identification of ASAH1 as a susceptibility gene for familial keloids.
Santos-Cortez RLP, Hu Y, Sun F, Benahmed-Miniuk F, Tao J, Kanaujiya JK, Ademola S, Fadiora S, Odesina V, Nickerson DA, Bamshad MJ, Olaitan PB, Oluwatosin OM, Leal SM, Reichenberger EJ. Santos-Cortez RLP, et al. Among authors: oluwatosin om. Eur J Hum Genet. 2017 Oct;25(10):1155-1161. doi: 10.1038/ejhg.2017.121. Epub 2017 Jul 26. Eur J Hum Genet. 2017. PMID: 28905881 Free PMC article.
Pediatric keloids: A 6-year retrospective review.
Michael AI, Ademola SA, Olawoye OA, Iyun AO, Adebayo W, Oluwatosin OM. Michael AI, et al. Among authors: oluwatosin om. Pediatr Dermatol. 2017 Nov;34(6):673-676. doi: 10.1111/pde.13302. Epub 2017 Oct 11. Pediatr Dermatol. 2017. PMID: 29023993
44 results