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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: lustosa mendes e. 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.
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: lustosa mendes e. 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
Pure 21q22.3 deletion identified in a patient with mild phenotypic features.
Sgardioli IC, Copelli MM, Lustosa-Mendes E, Vieira TP, Gil-da-Silva-Lopes VL. Sgardioli IC, et al. Among authors: lustosa mendes e. Congenit Anom (Kyoto). 2018 Sep;58(5):178-180. doi: 10.1111/cga.12270. Epub 2018 Feb 1. Congenit Anom (Kyoto). 2018. PMID: 29322562 No abstract available.
A Rare Case of Concomitant Deletions in 15q11.2 and 19p13.3.
Sgardioli IC, Lustosa-Mendes E, Dos Santos AP, Vieira TP, Gil-da-Silva-Lopes VL. Sgardioli IC, et al. Among authors: lustosa mendes e. Cytogenet Genome Res. 2018;156(2):80-86. doi: 10.1159/000493283. Epub 2018 Oct 9. Cytogenet Genome Res. 2018. PMID: 30296781
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. 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.
12 results