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Ocular and craniofacial phenotypes in a large Brazilian family with congenital aniridia.
Fernandes-Lima ZS, Paixão-Côrtes VR, Andrade AK, Fernandes AS, Coronado BN, Monte Filho HP, Santos MJ, Omena Filho RL, Biondi FC, Ruiz-Linares A, Ramallo V, Hünemeier T, Schuler-Faccini L, Monlleó IL. Fernandes-Lima ZS, et al. Among authors: monlleo il. Clin Genet. 2015;87(1):68-73. doi: 10.1111/cge.12329. Epub 2014 Jan 16. Clin Genet. 2015. PMID: 24266705
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: monlleo il. 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: monlleo il. 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.
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: monlleo il. Genes (Basel). 2024 Apr 21;15(4):518. doi: 10.3390/genes15040518. Genes (Basel). 2024. PMID: 38674452 Free PMC article.
32 results