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Preview	Issue Date	Title	Author(s)
	1997	A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome	Muenke, 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.
	1997	Mutations among Italian mucopolysaccharidosis Type I patients	Gatti, R.; Di Natale, P.; Villani, G.; Filocamo, M.; Muller, V.; Guo, X.H.; Nelson, P.; Scott, H.; Hopwood, J.
	1997	An in vitro study of silicone migration from intravenous fluid tubing	Dewan, P.; Owen, A.; Ashwood, P.; Terlet, J.; Byard, R.
	1997	Tandem balloon dilatation for childhood achalasia	Hammond, P.; Moore, D.; Davidson, G.; Davies, R.
	1997	Childhood cancer - a two-year prospective study of the psychological adjustment of children and parents	Sawyer, M.; Antoniou, G.; Toogood, I.; Rice, M.
	1997	Renal cystic disease in tuberous sclerosis: role of the polycystic kidney disease 1 gene	Sampson, J.; Maheshwar, M.; Aspinwall, R.; Thompson, P.; Cheadle, J.; Ravine, D.; Roy, S.; Haan, E.; Bernstein, J.; Harris, P.
	1997	Molecular defects in Sanfilippo syndrome type A	Blanch, L.; Weber, B.; Guo, X.H.; Scott, H.; Hopwood, J.
	1997	The spectrum of primary immundeficiency disorders in Australia	Baumgart, K.; Britton, W.; Kemp, A.; French, M.; Roberton, D.
	1997	Clinical features in four patients with Angelman syndrome resulting from paternal uniparental disomy	Smith, A.; Marks, R.; Haan, E.; Dixon, J.; Trent, R.
	1997	Power spectral analysis of heart rate variability in children and adolescents with IDDM	Wawryk, A.; Bates, D.; Couper, J.