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PreviewIssue DateTitleAuthor(s)
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.
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.
2008Nilotinib (formerly AMN107), a highly selective BCR-ABL tyrosine kinase inhibitor, is active in patients with imatinib-resistant or -intolerant accelerated-phase chronic myelogenous leukemiale Coutre, P.; Ottmann, O.; Giles, F.; Kim, D.; Cortes, J.; Gattermann, N.; Apperley, J.; Larson, R.; Abruzzese, E.; O'Brien, S.; Kuliczkowski, K.; Hochhaus, A.; Mahon, F.; Saglio, G.; Gobbi, M.; Kwong, Y.; Baccarani, M.; Hughes, T.; Martinelli, G.; Radich, J.; et al.
2008Identifying genetic traces of historical expansions: Phoenician footprints in the MediterraneanZalloua, P.; Platt, D.; El Sibai, M.; Khalife, J.; Makhoul, N.; Haber, M.; Xue, Y.; Izaabel, H.; Bosch, E.; Adams, S.; Arroyo, E.; Lopez-Parra, A.; Aler, M.; Picornell, A.; Ramon, M.; Jobling, M.; Comas, D.; Bertranpetit, J.; Spencer Wells, R.; Tyler-Smith, C.; et al.; Cooper, Alan
2008Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardationFroyen, G.; Corbett, M.; Vandewalle, J.; Jarvela, I.; Lawrence, O.; Meldrum, C.; Bauters, M.; Govaerts, K.; Vandeleur, L.; Van Esch, H.; Chelly, J.; Sanlaville, D.; van Bokhoven, H.; Ropers, H.; Laumonnier, F.; Ranieri, E.; Schwartz, C.; Abidi, F.; Tarpey, P.; Futreal, P.; et al.
2008Y-chromosomal diversity in Lebanon is structured by recent historical eventsZalloua, P.; Xue, Y.; Khalife, J.; Makhoul, N.; Debiane, L.; Platt, D.; Royyuru, A.; Herrera, R.; Hernanz, D.; Blue-Smith, J.; Spencer Wells, R.; Comas, D.; Bertranpetit, J.; Tyler-Smith, C.; Schurr, T.; Santos, F.; Quintana-Murci, L.; Balanovska, E.; Balanovsky, O.; Behar, D.; et al.; Cooper, Alan
2008Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosisBerkovic, S.; Dibbens, L.; Oshlack, A.; Silver, J.; Katerelos, M.; Vears, D.; Lullmann-Rauch, R.; Blanz, J.; Zhang, K.; Stankovich, J.; Kalnins, R.; Dowling, J.; Andermann, E.; Andermann, F.; Faldini, E.; D'Hooge, R.; Vadlamudi, L.; Macdonnell, R.; Hodgson, B.; Bayly, M.; et al.
2008SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndromeGilfillan, G.; Selmer, K.; Roxrud, I.; Smith, R.; Kyllerman, M.; Eiklid, K.; Kroken, M.; Mattingsdal, M.; Egeland, T.; Stenmark, H.; Sjoholm, H.; Server, A.; Samuelsson, L.; Christianson, A.; Tarpey, P.; Whibley, A.; Stratton, M.; Futreal, P.; Teague, J.; Edkins, S.; et al.
2008Comparison of twin and autologous transplants for multiple myelomaBashey, A.; Perez, W.; Zhang, M.; Anderson, K.; Ballen, K.; Berenson, J.; To, L.; Fonseca, R.; Freytes, C.; Gale, R.; Gibson, J.; Giralt, S.; Kyle, R.; Lazarus, H.; Maharaj, D.; McCarthy, P.; Milone, G.; Nimer, S.; Pavlovsky, S.; Reece, D.; et al.
2008Genome analysis of the platypus reveals unique signatures of evolutionWarren, W.; Hillier, L.; Graves, J.; Birney, E.; Ponting, C.; Grutzner, F.; Belov, K.; Miller, W.; Clarke, L.; Chinwall, A.; Yang, S.; Heger, A.; Locke, D.; Miethke, P.; Waters, P.; Veyrunes, F.; Fulton, L.; Fulton, B.; Graves, T.; Wallis, J.; et al.

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