Browsing by Author Vieira, TP

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Showing results 1 to 5 of 5
PreviewIssue DateTitleAuthor(s)AdvisorType
2013Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literatureMonteiro, FP; Vieira, TP; Sgardioli, IC; Molck, MC; Damiano, AP; Souza, J; Monlleo, IL; Fontes, MIB; Fett-Conte, AC; Felix, TM; Leal, GF; Ribeiro, EM; Banzato, CEM; Dantas, CD; Lopes-Cendes, I; Gil-da-Silva-Lopes, VL-Artigo de periódico
2013Partial 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 delaydos Santos, AP; Vieira, TP; Simioni, M; Monteiro, FP; Gil-da-Silva-Lopes, VL-Artigo de periódico
2013Atypical copy number abnormalities in 22q11.2 region: Report of three casesMolck, MC; Vieira, TP; Sgardioli, IC; Simioni, M; dos Santos, AP; Souza, J; Monteiro, FP; Gil-da-Silva-Lopes, VL-Artigo de periódico
2010Investigation of the 22q11.2 candidate region in patients with midline facial defects with hypertelorismSimioni, M; Freitas, EL; Vieira, TP; Lopes-Cendes, I; Gil-da-Silva-Lopes, VL-Artigo de periódico
2011Maternally Inherited Partial Monosomy 9p (pter -> p24.1) and Partial Trisomy 20p (pter -> p12.1) Characterized by Microarray Comparative Genomic HybridizationFreitas, EL; Gribble, SM; Simioni, M; Vieira, TP; Silva-Grecco, RL; Balarin, MAS; Prigmore, E; Krepischi-Santos, AC; Rosenberg, C; Szuhai, K; van Haeringen, A; Carter, NP; Gil-da-Silva-Lopes, VL-Artigo de periódico