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Preview	Issue Date	Title	Author(s)
	1998	Autosomal dominant Klippel-Feil anomaly with cleft palate	Thompson, E.; Haan, E.; Sheffield, L.
	1998	SHORT syndrome: distinctive radiographic features	Haan, E.; Morris, L.
	1998	IgG subclass antibodies to glutamic acid decarboxylase and risk for progression to clinical insulin-dependent diabetes	Couper, J.; Harrison, L.; Aldis, J.; Colman, P.; Honeyman, M.; Ferrante, A.
	1999	The role of family for behavioural outcome in children and adolescents following traumatic brain injury.	Kinsella, G.; Prior, M.; Murtagh, D.; Ong, B.; Sawyer, M.
	1995	Topography of axonal injury as defined by amyloid precursor protein and the sector scoring method in mild and severe closed head injury	Blumbergs, P.; Scott, G.; Manavis, J.; Wainwright, H.; Simpson, D.; McLean, J.
	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	The spectrum of primary immundeficiency disorders in Australia	Baumgart, K.; Britton, W.; Kemp, A.; French, M.; Roberton, D.
	1996	Intraorbital tissue expansion in the management of congenital anophthalmos	Dunaway, D.; David, D.
	1996	A novel X-linked gene, G4.5. is responsible for Barth Syndrome	Bione, S.; D'Adamo, P.; Maestrini, E.; Gedeon, A.; Bolhuis, P.; Toniolo, D.
	1995	Longitudinal evaluation of serum trypsinogen measurement in pancreatic-insufficient and pancreatic-sufficient patients with cystic fibrosis	Couper, R.; Corey, M.; Durie, P.; Forstner, G.; Moore, D.