Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Livro
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Oxford learner's pocket dictionary English-Greek, Greek-EnglishD. N. StavropoulosOxford Oxford University Press 1991Localização: FFLCH - Fac. Fil. Let. e Ciências Humanas (R489.32 S819oL )(Acessar) |
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Material Type: Livro
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Oxford Greek-English learner's dictionaryD. N. Stavropoulos G. N StavropoulosOxford Oxford University Press 1988Localização: FFLCH - Fac. Fil. Let. e Ciências Humanas (R489.32 S819o )(Acessar) |
3 |
Material Type: Livro
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Oxford english-greek learner's dictionaryD. N. Stavropoulos A.S HornbyOxford Oxford University Press 1992Localização: FFLCH - Fac. Fil. Let. e Ciências Humanas (R489.32 S819ox e.2 )(Acessar) |
4 |
Material Type: Artigo
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Consensus Statement chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomaliesDavid T. Miller Margaret P Adam; Swaroop Aradhya; Leslie G Biesecker; Arthur R Brothman; Nigel P Carter; Deanna M Church; John, A Crolla; E Eichler; Charles J Epstein; W. Andrew Faucett; Lars Feuk; Jan M Friedman; Ada Hamosh; Laird Jackson; Erin B Kaminsky; Klaas Kok; Ian D Krantz; Robert H Kuhn; Charles Lee; James M Ostell; Carla Rosenberg; Stephen W Scherer; Nancy B Spinner; Dimitri J Stavropoulos; James H Tepperberg; Erik C Thorland; Joris R Vermeesch; Darrel J Waggoner; Michael S Watson; Christa Lese Martin; David H LedbetterThe American Journal of Human Genetics Cambridge v. 86 n. 5, p. 749-764, may 2010Cambridge 2010Item não circula. Consulte sua biblioteca.(Acessar) |
5 |
Material Type: Artigo
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Consensus Statement chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomaliesDavid T. Miller Margaret P Adam; Swaroop Aradhya; Leslie G Biesecker; Arthur R Brothman; Nigel P Carter; Deanna M Church; John, A Crolla; E Eichler; Charles J Epstein; W. Andrew Faucett; Lars Feuk; Jan M Friedman; Ada Hamosh; Laird Jackson; Erin B Kaminsky; Klaas Kok; Ian D Krantz; Robert H Kuhn; Charles Lee; James M Ostell; Carla Rosenberg; Stephen W Scherer; Nancy B Spinner; Dimitri J Stavropoulos; James H Tepperberg; Erik C Thorland; Joris R Vermeesch; Darrel J Waggoner; Michael S Watson; Christa Lese Martin; David H LedbetterThe American Journal of Human Genetics Cambridge v. 86 n. 5, p. 749-764, may 2010Cambridge 2010Item não circula. Consulte sua biblioteca.(Acessar) |
6 |
Material Type: Artigo
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Therapy of tuberculosis in mice by DNA vaccinationDouglas B. Lowrie Ricardo E Tascon; Vânia Luiza Deperon Bonato; Valeria Marcal Felix de Lima; Lúcia Helena Faccioli; Evangelos Stavropoulos; M. Joseph Colston; Robert G Hewinson; Karin Moelling; Célio Lopes SilvaNature London v. 400, p. 269-271, 1999London 1999Localização: FCFRP - Fac. Ciên. Farm. Ribeirão Preto (pcd 1070082 )(Acessar) |
7 |
Material Type: Artigo
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Therapy of tuberculosis in mice by DNA vaccinationDouglas B. Lowrie Ricardo E Tascon; Vânia Luiza Deperon Bonato; Valeria Marcal Felix de Lima; Lúcia Helena Faccioli; Evangelos Stavropoulos; M. Joseph Colston; Robert G Hewinson; Karin Moelling; Célio Lopes SilvaNature London v. 400, p. 269-271, 1999London 1999Localização: FCFRP - Fac. Ciên. Farm. Ribeirão Preto (pcd 1070082 )(Acessar) |
8 |
Material Type: Artigo
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Protocol for a Prospective, Observational Cost-effectiveness Analysis of Returning Secondary Findings of Genome Sequencing for Unexplained Suspected Genetic ConditionsUngar, Wendy J. ; Hayeems, Robin Z. ; Marshall, Christian R. ; Gillespie, Meredith K. ; Szuto, Anna ; Chisholm, Caitlin ; James Stavropoulos, D. ; Huang, Lijia ; Jarinova, Olga ; Wu, Vercancy ; Tsiplova, Kate ; Lau, Lynnette ; Lee, Whiwon ; Venkataramanan, Viji ; Sawyer, Sarah ; Mendoza-Londono, Roberto ; Somerville, Martin J. ; Boycott, Kym M.Clinical therapeutics, 2023-08, Vol.45 (8), p.702-709 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
9 |
Material Type: Artigo
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Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual DisabilityBorlot, Felippe ; Regan, Brigid M ; Bassett, Anne S ; Stavropoulos, D. James ; Andrade, Danielle MJAMA neurology, 2017-11, Vol.74 (11), p.1301-1311 [Periódico revisado por pares]United States: American Medical AssociationTexto completo disponível |
10 |
Material Type: Artigo
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NSD1 mutations generate a genome-wide DNA methylation signatureChoufani, S ; Cytrynbaum, C ; Chung, B H Y ; Turinsky, A L ; Grafodatskaya, D ; Chen, Y A ; Cohen, A S A ; Dupuis, L ; Butcher, D T ; Siu, M T ; Luk, H M ; Lo, I F M ; Lam, S T S ; Caluseriu, O ; Stavropoulos, D J ; Reardon, W ; Mendoza-Londono, R ; Brudno, M ; Gibson, W T ; Chitayat, D ; Weksberg, RNature communications, 2015-12, Vol.6 (1), p.10207-10207, Article 10207 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |