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Preview	Issue Date	Title	Author(s)
	2002	Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome	Lower, 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.
	2002	Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy	Stromme, P.; Mangelsdorf, M.; Shaw, M.; Lower, K.; Lewis, S.; Bruyere, H.; Lutcherath, V.; Gedeon, A.; Wallace, R.; Scheffer, I.; Turner, G.; Partington, M.; Frints, S.; Fryns, J.; Sutherland, G.; Mulley, J.; Gecz, J.
	2003	Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation	Kalscheuer, V.; Freude, K.; Musante, L.; Jensen, L.; Yntema, H.; Gecz, J.; Sefiani, A.; Hoffmann, K.; Moser, B.; Haas, S.; Gurok, U.; Haesler, S.; Aranda, B.; Nshedjan, A.; Tzschach, A.; Hartmann, N.; Roloff, T.; Shoichet, S.; Hagens, O.; Tao, J.; et al.
	2005	Maternal segregation of the Dutch preeclampsia locus at 10q22 with a new member of the winged helix gene family	van Dijk, M.; Mulders, J.; Poutsma, A.; Konst, A.; Lachmeijer, A.; Dekker, G.; Blankenstein, M.; Oudejans, C.
	2004	In the platypus a meiotic chain of ten sex chromosomes shares genes with the bird Z and mammal X chromosomes	Grutzner, F.; Rens, W.; Tsend-Ayush, E.; El-Mogharbel, N.; O'Brien, P.; Jones, R.; Ferguson-Smith, M.; Graves, J.
	2003	Extreme reversed sexual size dimorphism in the extinct New Zealand moa Dinornis	Bunce, M.; Worthy, T.; Ford, T.; Hoppitt, W.; Willerslev, E.; Drummond, A.; Cooper, A.
	2009	The genome sequence of Taurine cattle: a window to ruminant biology and evolution	Bovine Genome Sequencing and Analysis Consortium,; Elsik, C.; Tellam, R.; Worley, K.; Adelson, David Louis
	2006	ZNF674: A new Kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation	Lugtenberg, D.; Yntema, H.; Banning, M.; Oudakker, A.; Firth, H.; Willatt, L.; Raynaud, M.; Kleefstra, T.; Fryns, J.; Ropers, H.; Chelly, J.; Moraine, C.; Gecz, J.; van Reeuwijk, J.; Nabuurs, S.; de Vries, B.; Hamel, B.; de Brouwer, A.; van Bokhoven, H.
	2009	SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype	Spurlock, G.; Bennett, E.; Chuzhanova, N.; Thomas, N.; H-Ping, J.; Side, L.; Davies, S.; Haan, E.; Kerr, B.; Huson, S.; Upadhyaya, M.
	2003	Heterozygous recipient and donor HFE mutations associated with a hereditary haemochromatosis phenotype after liver transplantation	Wigg, A.; Harley, H.; Casey, G.