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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.
2001A whole genome scan for differences in recombination rates among three Bos taurus breedsThomsen, H.; Reinsch, N.; Xu, N.; Bennewitz, J.; Looft, C.; Grupe, S.; Kuhn, C.; Brockmann, G.; Schwerin, M.; Leyhe-Horn, B.; Hiendleder, S.; Erhardt, G.; Medjugorac, I.; Russ, I.; Forster, M.; Brenig, B.; Reinhardt, F.; Reents, R.; Blumel, J.; Averdunk, G.; et al.
2003Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardationBurdon, K.; McKay, J.; Sale, M.; Russell-Eggitt, I.; Mackey, D.; Wirth, G.; Elder, J.; Nicoll, A.; Clarke, M.; FitzGerald, L.; Stankovich, J.; Shaw, M.; Sharma, S.; Gajovic, S.; Gruss, P.; Ross, S.; Thomas, P.; Voss, A.; Thomas, T.; Gecz, J.; et al.
2002Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndromeLower, K.; Turner, G.; Kerr, B.; Mathews, K.; Shaw, M.; Gedeon, A.; Schelley, S.; Hoyme, H.; White, S.; Delatycki, M.; Lampe, A.; Clayton-Smith, J.; Stewart, H.; van Ravenswaay, C.; de Vries, B.; Cox, B.; Grompe, M.; Ross, S.; Thomas, P.; Mulley, J.; et al.
2007A physical map of the bovine genomeSnelling, W.; Chiu, R.; Schein, J.; Hobbs, M.; Abbey, C.; Adelson, D.; Aerts, J.; Bennett, G.; Bosdet, I.; Boussaha, M.; Brauning, R.; Caetano, A.; Costa, M.; Crawford, A.; Dalrymple, B.; Eggen, A.; Everts-van der Wind, A.; Floriot, S.; Gautier, M.; Gill, C.; et al.

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