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Page 1
22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity.
de Wallau MB, Xavier AC, Moreno CA, Kim CA, Mendes EL, Ribeiro EM, Oliveira A, Félix TM, Fett-Conte AC, Bonadia LC, Correia-Costa GR, Monlleó IL, Gil-da-Silva-Lopes VL, Vieira TP. de Wallau MB, et al. Among authors: ribeiro em. Genes (Basel). 2024 Apr 21;15(4):518. doi: 10.3390/genes15040518. Genes (Basel). 2024. PMID: 38674452 Free PMC article.
Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature.
Monteiro FP, Vieira TP, Sgardioli IC, Molck MC, Damiano AP, Souza J, Monlleó IL, Fontes MI, Fett-Conte AC, Félix TM, Leal GF, Ribeiro EM, Banzato CE, Dantas Cde R, Lopes-Cendes I, Gil-da-Silva-Lopes VL. Monteiro FP, et al. Among authors: ribeiro em. Eur J Pediatr. 2013 Jul;172(7):927-45. doi: 10.1007/s00431-013-1964-0. Epub 2013 Feb 26. Eur J Pediatr. 2013. PMID: 23440478
A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population.
de Araujo TK, Secolin R, Félix TM, de Souza LT, Fontes MÍ, Monlleó IL, de Souza J, Fett-Conte AC, Ribeiro EM, Xavier AC, de Rezende AA, Simioni M, Ribeiro-dos-Santos ÂK, dos Santos SE, Gil-da-Silva-Lopes VL. de Araujo TK, et al. Among authors: ribeiro dos santos ak, ribeiro em. J Craniomaxillofac Surg. 2016 Jan;44(1):16-20. doi: 10.1016/j.jcms.2015.07.026. Epub 2015 Aug 13. J Craniomaxillofac Surg. 2016. PMID: 26602496
CranFlow: An Application for Record-Taking and Management Through the Brazilian Database on Craniofacial Anomalies.
Volpe-Aquino RM, Monlleó IL, Lustosa-Mendes E, Mora AF, Fett-Conte AC, Félix TM, Xavier AC, Tonocchi R, Ribeiro EM, Pereira R, Boy da Silva RT, de Rezende AA, Cavalcanti DP, Gil-da-Silva-Lopes VL. Volpe-Aquino RM, et al. Among authors: ribeiro em. Birth Defects Res. 2018 Jan 15;110(1):72-80. doi: 10.1002/bdr2.1123. Epub 2017 Sep 26. Birth Defects Res. 2018. PMID: 28949457
Genomic imbalances in craniofacial microsomia.
Spineli-Silva S, Sgardioli IC, Dos Santos AP, Bergamini LL, Monlleó IL, Fontes MIB, Félix TM, Ribeiro EM, Xavier AC, Lustosa-Mendes E, Gil-da-Silva-Lopes VL, Vieira TP. Spineli-Silva S, et al. Among authors: ribeiro em. Am J Med Genet C Semin Med Genet. 2020 Dec;184(4):970-985. doi: 10.1002/ajmg.c.31857. Epub 2020 Nov 20. Am J Med Genet C Semin Med Genet. 2020. PMID: 33215817 Review.
Study of IRF6 and 8q24 region in non-syndromic oral clefts in the Brazilian population.
de Souza LT, Kowalski TW, Ferrari J, Monlléo IL, Ribeiro EM, de Souza J, Fett-Conte AC, de Araujo TK, Gil-da-Silva-Lopes VL, Ribeiro-Dos-Santos ÂK, dos Santos SE, Félix TM. de Souza LT, et al. Among authors: ribeiro dos santos ak, ribeiro em. Oral Dis. 2016 Apr;22(3):241-5. doi: 10.1111/odi.12432. Epub 2016 Feb 1. Oral Dis. 2016. PMID: 26714022
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: ribeiro em. 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.
Implementing the brazilian database on orofacial clefts.
Monlleó IL, Fontes MÍ, Ribeiro EM, de Souza J, Leal GF, Félix TM, Fett-Conte AC, Bueno BH, Magna LA, Mossey PA, Gil-da Silva-Lopes V. Monlleó IL, et al. Among authors: ribeiro em. Plast Surg Int. 2013;2013:641570. doi: 10.1155/2013/641570. Epub 2013 Mar 12. Plast Surg Int. 2013. PMID: 23577250 Free PMC article.
167 results