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Array-CGH analysis in patients with intellectual disability and/or congenital malformations in Brazil.
Genet Mol Res. 2016 Feb 19;15(1). doi: 10.4238/gmr.15017769.
Genet Mol Res. 2016.
PMID: 26909975
Free article.
Identifying CNVs in 15q11q13 and 16p11.2 of Patients with Seizures Increases the Rates of Detecting Pathogenic Changes.
Vianna GS, Freitas ML, Oliveira VT, Pietra RX, Gonçalves MD, Rocha PP, Monteiro RA, Ferreira LC, Xavier RR, Carvalho AM, Lima PR, Monteiro MA, Mateo EC, Giannetti JG, César GD, Lima JS, Medeiros PF, Jehee FS.
Vianna GS, et al.
Mol Syndromol. 2016 Nov;7(6):329-336. doi: 10.1159/000450631. Epub 2016 Nov 1.
Mol Syndromol. 2016.
PMID: 27920636
Free PMC article.
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Major Contribution of Genomic Copy Number Variation in Syndromic Congenital Heart Disease: The Use of MLPA as the First Genetic Test.
Monteiro RAC, de Freitas ML, Vianna GS, de Oliveira VT, Pietra RX, Ferreira LCA, Rocha PPO, da S Gonçalves M, da C César G, de S Lima J, Medeiros PFV, Mazzeu JF, Jehee FS.
Monteiro RAC, et al. Among authors: vianna gs.
Mol Syndromol. 2017 Aug;8(5):227-235. doi: 10.1159/000477226. Epub 2017 Jun 14.
Mol Syndromol. 2017.
PMID: 28878606
Free PMC article.
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Dual molecular diagnosis contributes to atypical Prader-Willi phenotype in monozygotic twins.
Jehee FS, de Oliveira VT, Gurgel-Giannetti J, Pietra RX, Rubatino FVM, Carobin NV, Vianna GS, de Freitas ML, Fernandes KS, Ribeiro BSV, Brüggenwirth HT, Ali-Amin R; Baylor-Hopkins Center for Mendelian Genomics; White JJ, Akdemir ZC, Jhangiani SN, Gibbs RA, Lupski JR, Varela MC, Koiffmann C, Rosenberg C, Carvalho CMB.
Jehee FS, et al. Among authors: vianna gs.
Am J Med Genet A. 2017 Sep;173(9):2451-2455. doi: 10.1002/ajmg.a.38315. Epub 2017 Jun 20.
Am J Med Genet A. 2017.
PMID: 28631899
Free PMC article.
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High-level mosaic monosomy 21 in a 13-year-old girl: Case report and review of the literature.
Viana MM, Vianna GS, Carvalho ERF, da Costa HBBLM, de Aguiar MJB.
Viana MM, et al. Among authors: vianna gs.
Am J Med Genet A. 2022 Mar;188(3):953-958. doi: 10.1002/ajmg.a.62583. Epub 2021 Dec 10.
Am J Med Genet A. 2022.
PMID: 34889506
Review.
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Are 22q11.2 distal deletions associated with math difficulties?
Carvalho MR, Vianna G, Oliveira Lde F, Costa AJ, Pinheiro-Chagas P, Sturzenecker R, Zen PR, Rosa RF, de Aguiar MJ, Haase VG.
Carvalho MR, et al.
Am J Med Genet A. 2014 Sep;164A(9):2256-62. doi: 10.1002/ajmg.a.36649. Epub 2014 Jul 2.
Am J Med Genet A. 2014.
PMID: 24989330
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Count on dopamine: influences of COMT polymorphisms on numerical cognition.
Júlio-Costa A, Antunes AM, Lopes-Silva JB, Moreira BC, Vianna GS, Wood G, Carvalho MR, Haase VG.
Júlio-Costa A, et al. Among authors: vianna gs.
Front Psychol. 2013 Aug 15;4:531. doi: 10.3389/fpsyg.2013.00531. eCollection 2013.
Front Psychol. 2013.
PMID: 23966969
Free PMC article.
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