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PreviewIssue DateTitleAuthor(s)
2002Recombinant Human Bone Morphogenetic Protein-2 for Treatment of Open Tibial FracturesCsimma, C.; Genant, H.; Valentin-Opran, A.; Amit, Y.; Arbel, R.; Aro, H.; Atar, D.; Bishay, M.; Borner, M.; Chiron, P.; Choong, P.; Cinats, J.; Courtenay, B.; Feibel, R.; Geulette, B.; Gravel, C.; Haas, N.; Raschke, M.; Hammacher, E.; van der Velde, D.; et al.
2004Rise and fall of the Beringian steppe bisonShapiro, B.; Drummond, A.; Rambaut, A.; Wilson, M.; Matheus, P.; Sher, A.; Pybus, O.; Gilbert, M.; Barnes, I.; Binladen, J.; Willerslev, E.; Hansen, A.; Baryshnikov, G.; Burns, J.; Davydov, S.; Driver, J.; Froese, D.; Harington, C.; Keddie, G.; Kosintsev, P.; et al.
2016CXCR5⁺ follicular cytotoxic T cells control viral infection in B cell folliclesLeong, Y.; Chen, Y.; Ong, H.; Wu, D.; Man, K.; Deleage, C.; Minnich, M.; Meckiff, B.; Wei, Y.; Hou, Z.; Zotos, D.; Fenix, K.; Atnerkar, A.; Preston, S.; Chipman, J.; Beilman, G.; Allison, C.; Sun, L.; Wang, P.; Xu, J.; et al.
2008X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentDibbens, L.; Tarpey, P.; Hynes, K.; Bayly, M.; Scheffer, I.; Smith, R.; Bomar, J.; Sutton, E.; Vandeleur, L.; Shoubridge, C.; Edkins, S.; Turner, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Jones, D.; et al.
2001Integration of cytogenetic landmarks into the draft sequence of the human genomeCheung, V.; Nowak, N.; Jang, W.; Kirsch, I.; Zhao, S.; Chen, X.; Furey, T.; Kim, U.; Kuo, W.; Olivier, M.; Conroy, J.; Kasprzyk, A.; Massa, H.; Yonescu, R.; Sait, S.; Thoreen, C.; Snijders, A.; Lemyre, E.; Bailey, J.; Bruzel, A.; et al.
2008The global network on dental education: a new vision for IFDEAde Vries, J.; Murtomaa, H.; Butler, M.; Cherrett, H.; Ferrillo, P.; Ferro, M.; Gadbury-Amyot, C.; Haden, N.; Manogue, M.; Mintz, J.; Mulvihill, J.; Murray, B.; Nattestad, A.; Nielsen, D.; Ogunbodede, E.; Parkash, H.; Plasschaert, F.; Reed, M.; Rupp, R.; Tandon, S.; et al.
1995An integrated physical map of human chromosome 16Doggett, N.; Goodwin, L.; Tesmer, J.; Meincke, L.; Bruce, D.; Clark, L.; Altherr, M.; Ford, A.; Chi, H.C.; Marrone, B.; Longmire, J.; Lane, S.; Whitmore, S.; Lowenstein, N.; Sutherland, G.; Mundt, M.; Knill, E.; Bruno, W.; Macken, C.; Torney, D.; et al.
2007Epidemiological comparisons of problems and positive qualities reported by adolescents in 24 countriesRescorla, L.; Achenbach, T.; Ivanova, M.; Dumenci, L.; Almqvist, F.; Bilenberg, N.; Bird, H.; Broberg, A.; Dobrean, A.; Dopfner, M.; Erol, N.; Forns, M.; Hannesdottir, H.; Kanbayashi, Y.; Lambert, M.; Leung, P.; Minaei, A.; Mulatu, M.; Novik, T.; Oh, K.; et al.
1997A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndromeMuenke, M.; Gripp, K.; McDonald-McGinn, D.; Gaudenz, K.; Whitaker, L.; Bartlett, S.; Markowitz, R.; Robin, N.; Nwokoro, N.; Mulvihill, J.; Losken, H.; Mulliken, J.; Guttmacher, A.; Wilroy, R.; Clarke, L.; Hollway, G.; Ades, L.; Haan, E.; Mulley, J.; Cohen, M.; et al.
2004Interlaboratory comparison of results of susceptibility testing with caspofungin against candida and aspergillus speciesOdds, F.; Motyl, M.; Andrade, R.; Bille, J.; Canton, E.; Cuenca-Estrella, M.; Davidson, A.; Durussel, C.; Ellis, D.; Foraker, E.; Fothergill, A.; Ghannoum, M.; Giacobbe, R.; Gobernado, M.; Handke, R.; Laverdiere, M.; Lee-Yang, W.; Merz, W.; Ostrosky-Zeichner, L.; Peman, J.; et al.

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