Browsing by Author Sgardioli, IC

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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
2013A new case of partial 14q31.3-qter trisomy due to maternal pericentric inversionSgardioli, IC; Simioni, M; Viguetti-Campos, NL; Prota, JR; 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
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