Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Recurso Textual
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Spreekwoorden in beeld een aparte kunst uit CabindaJan VissersBerg en Dal Afrika Museum 1989Localização: MAE - Museu Arqueologia e Etnologia (FOL3548 )(Acessar) |
2 |
Material Type: Artigo de Congresso
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Profiling of The Known-Unknowns Passiflora Complement by Liquid Chromatography - Ion Mobility - Mass SpectrometryMichael McCullagh Jeff Goshawk; Russell J Mortishire-Smith; Cintia AM Pereira; Janete Harumi Yariwake; Johannes PC Vissers; AOAC International Annual Meeting & Exposition 2020 DallasWaters STEM Ambassador Gaithersburg : AOAC International, 2020Gaithersburg AOAC International 2020Localização: IQSC - Inst. Química de São Carlos (P19007 ) e outros locais(Acessar) |
3 |
Material Type: Artigo
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Profiling of the known-unknown Passiflora variant complement by liquid chromatography - Ion mobility - Mass spectrometryMichael McCullagh Jeff Goshawk; David Eatough; Russell J Mortishire-Smith; Cintia A. M Pereira; Janete Harumi Yariwake; Johannes PC VissersTalanta Amsterdam : Elsevier BV v. 221, n. 1, p. 121311 2021Amsterdam 2021Localização: IQSC - Inst. Química de São Carlos (P18947 )(Acessar) |
4 |
Material Type: Livro
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LOTOSphere: Software Development with LOTOSTommaso van de Lagemaat, Jeroen Vissers, Chris Bolognesi Jeroen van de Lagemaat; Chris VissersSpringer US 1995Acesso online |
5 |
Material Type: Livro
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6 |
Material Type: Livro
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A Corpus of Rembrandt PaintingsBruyn D Cook-Radmore; B Haak; S. H Levie; L Peese Binkhorst-Hoffscholte; E van de Wetering; P. J. J van Thiel; J VisSpringer Netherlands 1989Acesso online |
7 |
Material Type: Artigo
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Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD. A. Koolen A. J Sharp; J. A Hurst; Helen V Firth; S. J. L Knight; A Goldenberg; P Saugier-Veber; R Pfundt; L. E. L. M Vissers; A Destrée; B Grisart; L Rooms; N Van der Aa; M Field; A Hackett; K Bell; M. J. M Nowaczyk; G. M. S Mancini; P. J Poddighe; C. E Schwartz; E Rossi; M De Gregori; L. L Antonacci-Fulton; M. D McLellan II; J. M Garrett; M A Wiechert; T. L Miner; S Crosby; R Ciccone; Lionel Willatt; A Rauch; Martin Zenker; S Aradhya; M. A Manning; T. M Strom; J Wagenstaller; Ana Cristina Victorino Krepischi; Angela M Vianna-Morgante; Carla Rosenberg; S. M Price; H Stewart; Charles Shaw-Smith; H. G Brunner; A. O. M Wilkie; J. A Veltman; O Zuffardi; E. E Eichler; B. B. A VriesJournal of Medical Genetics v. 45, n. 11, p. 710-720, 2008London 2008Item não circula. Consulte sua biblioteca.(Acessar) |
8 |
Material Type: Artigo
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Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD. A. Koolen A. J Sharp; J. A Hurst; Helen V Firth; S. J. L Knight; A Goldenberg; P Saugier-Veber; R Pfundt; L. E. L. M Vissers; A Destrée; B Grisart; L Rooms; N Van der Aa; M Field; A Hackett; K Bell; M. J. M Nowaczyk; G. M. S Mancini; P. J Poddighe; C. E Schwartz; E Rossi; M De Gregori; L. L Antonacci-Fulton; M. D McLellan II; J. M Garrett; M A Wiechert; T. L Miner; S Crosby; R Ciccone; Lionel Willatt; A Rauch; Martin Zenker; S Aradhya; M. A Manning; T. M Strom; J Wagenstaller; Ana Cristina Victorino Krepischi-Santos; Angela Maria Vianna-Morgante; Carla Rosenberg; S. M Price; H Stewart; Charles Shaw-Smith; H. G Brunner; A. O. M Wilkie; J. A Veltman; O Zuffardi; E. E Eichler; B. B. A VriesJournal of Medical Genetics v. 45, n. 11, p. 710-720, 2008London 2008Item não circula. Consulte sua biblioteca.(Acessar) |
9 |
Material Type: Artigo
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Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and miceLisenka E. L. M. Vissers Timothy C Cox; A. Murat Maga; Kieran M Short; Fenny Wiradjaja; Irene M Janssen; Fernanda Sarquis Jehee; Débora Romeo Bertola; Jia Liu; Garima Yagnik; Kiyotoshi Sekiguchi; Daiji Kiyozumi; Hans van Bokhoven; Carlo Marcelis; Michael Cunningham; Peter J Anderson; Simeon A Boyadjiev; Maria Rita Passos-Bueno; Joris A Veltman; Ian Smyth; Michael F Buckley; Tony RoscioliPLoS Genetics San Francisco v. 7, n, 9, p. e1002278, sept. 2011San Francisco 2011Item não circula. Consulte sua biblioteca.(Acessar) |
10 |
Material Type: Artigo
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Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and miceLisenka E. L. M. Vissers Timothy C Cox; A. Murat Maga; Kieran M Short; Fenny Wiradjaja; Irene M Janssen; Fernanda Sarquis Jehee; Débora Romeo Bertola; Jia Liu; Garima Yagnik; Kiyotoshi Sekiguchi; Daiji Kiyozumi; Hans van Bokhoven; Carlo Marcelis; Michael Cunningham; Peter J Anderson; Simeon A Boyadjiev; Maria Rita Passos-Bueno; Joris A Veltman; Ian Smyth; Michael F Buckley; Tony RoscioliPLoS Genetics San Francisco v. 7, n, 9, p. e1002278, sept. 2011San Francisco 2011Item não circula. Consulte sua biblioteca.(Acessar) |