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Partial 1q Duplications and Associated Phenotype.
Morris ML, Baroneza JE, Teixeira P, Medina CT, Cordoba MS, Versiani BR, Roese LL, Freitas EL, Fonseca AC, Dos Santos MC, Pic-Taylor A, Rosenberg C, Oliveira SF, Ferrari I, Mazzeu JF. Morris ML, et al. Among authors: ferrari i. Mol Syndromol. 2016 Feb;6(6):297-303. doi: 10.1159/000443599. Epub 2016 Feb 4. Mol Syndromol. 2016. PMID: 27022331 Free PMC article.
Complex phenotype associated with 17q21.31 microdeletion.
Dornelles-Wawruk H, Pic-Taylor A, Rosenberg C, Krepischi AC, Safatle HP, Ferrari I, Mazzeu JF. Dornelles-Wawruk H, et al. Among authors: ferrari i. Mol Syndromol. 2013 Sep;4(6):297-301. doi: 10.1159/000354120. Epub 2013 Aug 21. Mol Syndromol. 2013. PMID: 24167466 Free PMC article.
Concurrent Loss of Heterozygosity and Mosaic Deletion of 12p13.32pter.
Faria RS, de Oliveira CP, da Costa MM, da S Rosa MT, Córdoba MS, Pic-Taylor A, Ferrari I, de Oliveira SF, Mazzeu JF. Faria RS, et al. Among authors: ferrari i. Cytogenet Genome Res. 2016;148(2-3):174-8. doi: 10.1159/000445853. Epub 2016 Jun 2. Cytogenet Genome Res. 2016. PMID: 27251740
Does celiac disease occur in Afro-derived Brazilian populations?
Almeida RC, Gandolfi L, De Nazaré Klautau-Guimarães M, Ferrari I, Sousa SM, Abe-Sandes K, Barbosa AA, Simões AL, Pratesi R, Oliveira SF. Almeida RC, et al. Among authors: ferrari i. Am J Hum Biol. 2012 Sep-Oct;24(5):710-2. doi: 10.1002/ajhb.22271. Epub 2012 Apr 17. Am J Hum Biol. 2012. PMID: 22508149
Exclusion of Class III malocclusion candidate loci in Brazilian families.
Cruz RM, Hartsfield JK Jr, Falcão-Alencar G, Koller DL, Pereira RW, Mah J, Ferrari I, Oliveira SF. Cruz RM, et al. Among authors: ferrari i. J Dent Res. 2011 Oct;90(10):1202-5. doi: 10.1177/0022034511416668. Epub 2011 Aug 1. J Dent Res. 2011. PMID: 21810622 Free PMC article.
218 results