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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 2
2004 3
2005 1
2006 7
2007 3
2008 1
2009 1
2010 1
2011 3
2012 6
2013 7
2014 5
2015 5
2016 4
2017 2
2018 5
2019 4
2020 4
2021 1
2022 6
2023 4
2024 6

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70 results

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Page 1
Risk factors and the prevention of oral clefts.
Gil-da-Silva-Lopes VL, Monlleo IL. Gil-da-Silva-Lopes VL, et al. Braz Oral Res. 2014;28 Spec No:1-5. doi: 10.1590/S1806-83242014.50000008. Epub 2014 Feb 12. Braz Oral Res. 2014. PMID: 24554096 Free article. Review.
Syndromic Retinitis Pigmentosa: A 15-Patient Study.
Holanda IP, Rim PHH, Rare Genomes Project Consortium, Guaragna MS, Gil-da-Silva-Lopes VL, Steiner CE. Holanda IP, et al. Among authors: gil da silva lopes vl. Genes (Basel). 2024 Apr 20;15(4):516. doi: 10.3390/genes15040516. Genes (Basel). 2024. PMID: 38674450 Free PMC article.
Identification of genomic imbalances in oral clefts.
Lustosa-Mendes E, Santos APD, Vieira TP, Ribeiro EM, Rezende AA, Fett-Conte AC, Cavalcanti DP, Félix TM, Monlleó IL, Gil-da-Silva-Lopes VL. Lustosa-Mendes E, et al. Among authors: gil da silva lopes vl. J Pediatr (Rio J). 2021 May-Jun;97(3):321-328. doi: 10.1016/j.jped.2020.06.005. Epub 2020 Jul 21. J Pediatr (Rio J). 2021. PMID: 32707036 Free PMC article.
Demographic history differences between Hispanics and Brazilians imprint haplotype features.
da Cruz PRS, Ananina G, Secolin R, Gil-da-Silva-Lopes VL, Lima CSP, de França PHC, Donatti A, Lourenço GJ, de Araujo TK, Simioni M, Lopes-Cendes I, Costa FF, de Melo MB. da Cruz PRS, et al. Among authors: gil da silva lopes vl. G3 (Bethesda). 2022 Jul 6;12(7):jkac111. doi: 10.1093/g3journal/jkac111. G3 (Bethesda). 2022. PMID: 35511163 Free PMC article.
Genomic imbalances in syndromic congenital heart disease.
Molck MC, Simioni M, Paiva Vieira T, Sgardioli IC, Paoli Monteiro F, Souza J, Fett-Conte AC, Félix TM, Lopes Monlléo I, Gil-da-Silva-Lopes VL. Molck MC, et al. Among authors: gil da silva lopes vl. J Pediatr (Rio J). 2017 Sep-Oct;93(5):497-507. doi: 10.1016/j.jped.2016.11.007. Epub 2017 Mar 21. J Pediatr (Rio J). 2017. PMID: 28336264 Free article.
A recognizable phenotype related to 19p13.12 microdeletion.
de Souza LC, Sgardioli IC, Gil-da-Silva-Lopes VL, Vieira TP. de Souza LC, et al. Among authors: gil da silva lopes vl. Am J Med Genet A. 2018 Aug;176(8):1753-1759. doi: 10.1002/ajmg.a.38842. Epub 2018 Jul 28. Am J Med Genet A. 2018. PMID: 30055032
70 results