Gil-da-Silva-Lopes VL - Search Results

1

17p13.3 Microdeletion: Insights on Genotype-Phenotype Correlation.

Barros Fontes MI, Dos Santos AP, Rossi Torres F, Lopes-Cendes I, Cendes F, Appenzeller S, Kawasaki de Araujo T, Lopes Monlleó I, Gil-da-Silva-Lopes VL. Barros Fontes MI, et al. Mol Syndromol. 2017 Jan;8(1):36-41. doi: 10.1159/000452753. Epub 2016 Nov 25. Mol Syndromol. 2017. PMID: 28232781 Free PMC article.

2

How are people with orofacial clefts attended in northwest region of São Paulo state, Brazil?

Francisquetti MCC, Gil-da-Silva-Lopes VL, Fett-Conte AC. Francisquetti MCC, et al. Among authors: gil da silva lopes vl. Genet Mol Biol. 2023 Dec 18;46(4):e20230167. doi: 10.1590/1678-4685-GMB-2023-0167. eCollection 2023. Genet Mol Biol. 2023. PMID: 38112488 Free PMC article.

3

Midline facial defects with hypertelorism and low-grade astrocytoma: a previously undescribed association.

Giffoni SD, Cendes F, Valente M, Gil-da-Silva-Lopes VL. Giffoni SD, et al. Cleft Palate Craniofac J. 2006 Nov;43(6):748-51. doi: 10.1597/05-099. Cleft Palate Craniofac J. 2006. PMID: 17105323

4

Investigation of the 22q11.2 candidate region in patients with midline facial defects with hypertelorism.

Simioni M, Freitas EL, Vieira TP, Lopes-Cendes I, Gil-da-Silva-Lopes VL. Simioni M, et al. J Appl Genet. 2010;51(2):219-21. doi: 10.1007/BF03195732. J Appl Genet. 2010. PMID: 20453311

5

Malformations of cortical development in patients with midline facial defects and ocular hypertelorism.

Giffoni SD, Cendes F, Valente M, Gil-da-Silva-Lopes VL. Giffoni SD, et al. Cleft Palate Craniofac J. 2010 Jul;47(4):343-51. doi: 10.1597/08-167.1. Cleft Palate Craniofac J. 2010. PMID: 20590457

6

Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia.

Simioni M, Vieira TP, Sgardioli IC, Freitas EL, Rosenberg C, Maurer-Morelli CV, Lopes-Cendes I, Fett-Conte AC, Gil-da-Silva-Lopes VL. Simioni M, et al. Am J Med Genet A. 2012 Nov;158A(11):2905-10. doi: 10.1002/ajmg.a.35603. Epub 2012 Sep 18. Am J Med Genet A. 2012. PMID: 22991255

7

Partial monosomy 21 (q11.2→q21.3) combined with 3p25.3→pter monosomy due to an unbalanced translocation in a patient presenting dysmorphic features and developmental delay.

dos Santos AP, Vieira TP, Simioni M, Monteiro FP, Gil-da-Silva-Lopes VL. dos Santos AP, et al. Gene. 2013 Jan 25;513(2):301-4. doi: 10.1016/j.gene.2012.09.008. Epub 2012 Sep 29. Gene. 2013. PMID: 23031812 Free article.

8

Preliminary Analysis of the Nonsynonymous Polymorphism rs17563 in BMP4 Gene in Brazilian Population Suggests Protection for Nonsyndromic Cleft Lip and Palate.

Araújo TK, Simioni M, Félix TM, de Souza LT, Fontes MÍ, Monlleó IL, Souza J, Fett-Conte AC, Secolin R, Lopes-Cendes I, Maurer-Morelli CV, Gil-da-Silva-Lopes VL. Araújo TK, et al. Plast Surg Int. 2012;2012:247104. doi: 10.1155/2012/247104. Epub 2012 Nov 27. Plast Surg Int. 2012. PMID: 23227324 Free PMC article.

9

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. 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

10

Atypical copy number abnormalities in 22q11.2 region: report of three cases.

Molck MC, Vieira TP, Sgardioli IC, Simioni M, Dos Santos AP, Souza J, Monteiro FP, Gil-da-Silva-Lopes VL. Molck MC, et al. Eur J Med Genet. 2013 Sep;56(9):515-20. doi: 10.1016/j.ejmg.2013.07.002. Epub 2013 Jul 23. Eur J Med Genet. 2013. PMID: 23886712 Free article.

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