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Preview	Issue Date	Title	Author(s)
	1998	Coexistence of Gaucher-Disease Type 1 and Joubert-Syndrome	Van Royen-Kerkhof, A.; Pollthe, B.; Kleijer, W.; van Diggelen, O.; Aerts, J.; Hopwood, J.; Beemer, F.
	1998	Febrile seizures and generalised epilepsy associated with a mutation in the Na+-channel b1 subunit gene SCN1B	Wallace, R.; Wang, D.; Singh, R.; Scheffer, I.; George Jnr., A.; Phillips, H.; Saar, K.; Reis, A.; Johnson, E.; Sutherland, G.; Berkovic, S.; Mulley, J.
	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.
	1998	Autosomal dominant Klippel-Feil anomaly with cleft palate	Thompson, E.; Haan, E.; Sheffield, L.
	1998	Gene localisation for an autosomal dominant familial periodic fever to 12p13.	Mulley, J.; Saar, K.; Hewitt, G.; Rueschendorf, F.; Phillips, H.; Colley, A.; Sillence, D.; Reis, A.; Wilson, M.
	1998	CAG repeat expansion in autosomal dominant familial spastic paraparesis - novel expansion in a subset of patients	Benson, K.; Horwitz, M.; Wolff, J.; Friend, K.; Thompson, E.; White, S.; Richards, R.; Raskind, W.; Bird, T.
	1998	Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16	Cavanaugh, J.; Callen, D.; Wilson, S.; Stanford, P.; Sraml, M.; Gorska, M.; Crawford, J.; Whitmore, S.; Shlegel, C.; Foote, S.; Kohonen-Corish, M.; Pavli, P.
	1998	A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis.	Town, M.; Jean, G.; Cherqui, S.; Attard, M.; Forestier, L.; Whitmore, S.; Callen, D.; Gribouval, O.; Broyer, M.; Bates, G.; van't Hoff, W.; Antignac, C.
	1998	Two mutations within a feline mucopolysaccharidosis type VI colony cause three different clinical phenotypes	Crawley, A.; Yogalingam, G.; Muller, V.; Hopwood, J.
	1998	PAK3 mutation in nonsyndromic X-linked mental retardation	Allen, K.; Gleeson, J.; Bagrodia, S.; Partington, M.; MacMillan, J.; Cerione, R.; Mulley, J.; Walsh, C.