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Preview	Issue Date	Title	Author(s)
	1998	Familial partial epilepsy with variable foci: A new partial epilepsy syndrome with suggestion of linkage to chromosome 2	Scheffer, I.; Phillips, H.; O'Brien, C.; Saling, M.; Wrennall, J.; Wallace, R.; Mulley, J.; Berkovic, S.
	1996	A 3-year follow-up of the intellectual and academic functioning of children receiving central nervous system prophylactic chemotherapy for leukemia	Brown, R.; Sawyer, M.; Antoniou, G.; Toogood, I.; Rice, M.; Thompson, N.; Madan-Swain, A.
	1998	Autosomal dominant Klippel-Feil anomaly with cleft palate	Thompson, E.; Haan, E.; Sheffield, L.
	1998	Bowel dysfunction in cystic fibrosis: importance of breath testing	Lewindon, P.; Robb, T.; Moore, D.; Davidson, G.; Martin, A.
	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.
	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.
	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.
	1999	Lung function outcome in children of premature birth [Review]	Kennedy, J.