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Preview	Issue Date	Title	Author(s)
	2000	The FMR2 gene, FRAXE and non-specific X-linked mental retardation: clinical and molecular aspects	Gecz, J.
	2005	Analysis of normal and mutant iduronate-2-sulphatase conformation	Parkinson-Lawrence, E.; Turner, C.; Hopwood, J.; Brooks, D.
	1999	Sanfilippo type B syndrome (mucopolysaccharidosis III B): allelic heterogeneity corresponds to the wide spectrum of clinical phenotypes	Weber, B.; Guo, X.H.; Kleijer, W.; van de Kamp, J.; Poorthuis, B.; Hopwood, J.
	2005	Neonatal epilepsy syndromes and generalized epilepsy with febrile seizures plus (GEFS+)	Scheffer, I.; Harkin, L.; Dibbens, L.; Mulley, J.; Berkovic, S.
	2003	Prevalence of mucopolysaccharidosis type VI mutations in Siamese cats	Crawley, A.; Muntz, F.; Haskins, M.; Jones, B.; Hopwood, J.
	2003	Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotype	Maxwell, M.; Bjorkman, J.; Nguyen, T.; Sharp, P.; Finnie, J.; Paterson, C.; Tonks, I.; Paton, B.; Kay, G.; Crane, D.
	1998	Mild feline mucopolysaccharidosis type VI. Identification of an N-acetylgalactosamine-4-sulfatase mutation causing instability and increased specific activity	Yogalingam, G.; Hopwood, J.; Crawley, A.; Anson, D.
	1998	Two mutations within a feline mucopolysaccharidosis type VI colony cause three different clinical phenotypes	Crawley, A.; Yogalingam, G.; Muller, V.; Hopwood, J.
	2014	Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth	Homan, C.; Kumar, R.; Nguyen, L.; Haan, E.; Raymond, F.; Abidi, F.; Raynaud, M.; Schwartz, C.; Wood, S.; Gecz, J.; Jolly, L.
	1998	Genotype-phenotype correlations in mucopolysaccharidosis type I using enzyme kinetics, immunoquantification and in vitro turnover studies	Bunge, S.; Clements, P.; Byers, S.; Kleijer, W.; Brooks, D.; Hopwood, J.