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Preview	Issue Date	Title	Author(s)
	1999	Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Börjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patient	Gecz, J.; Baker, E.; Donnelly, A.; Ming, J.; McDonald-McGinn, D.; Spinner, N.; Zackai, E.; Sutherland, G.; Mulley, J.
	1999	Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM	Friend, K.; Crimmins, D.; Phan, T.; Sue, C.; Colley, A.; Fung, V.; Morris, J.; Sutherland, G.; Richards, R.
	1999	A putative exchange factor for Rho1 GTPase is required for initiation of cytokinesis in Drosophila	Prokopenko, S.; Brumby, A.; O'Keefe, L.; Prior, L.; He, Y.; Saint, R.; Bellen, H.
	1998	Specific expression of an expansin gene during elongation of cotton fibres.	Orford, S.; Timmis, J.
	1999	DECAY, a novel Drosophila caspase related to mammalian Caspase-3 and Caspase-7	Dorstyn, L.; Read, S.; Quinn, L.; Richardson, H.; Kumar, S.
	1997	Ancient missense mutations in a new member of the RoRet gene family are likely to cause Familial Mediterranean Fever	Aksentijevich, I.; Centola, M.; Deng, Z.; Sood, R.; Balow, J.; Wood, G.; Zaks, N.; Mansfield, E.; Chen, X.; Eisenberg, S.; Vedula, A.; Shafran, N.; Raben, N.; Pras, E.; Pras, M.; Kastner, D.; Blake, T.; Baxevanis, A.; Robbins, C.; Krizman, D.; et al.
	1999	Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes	McDermott, M.; Aksentijevich, I.; Galon, J.; McDermott, E.; Ogunkolade, B.; Centola, M.; Mansfield, E.; Gadina, M.; Karenko, L.; Petterson, T.; McCarthy, J.; Frucht, D.; Aringer, M.; Torosyan, Y.; Teppo, A.M.; Wilson, M.; Karaarslan, H.; Wan, Y.; Todd, I.; Wood, G.; et al.
	1997	Pyruvate decarboxylase and anaerobic survival in Aspergillus nidulans	Lockington, R.; Borlace, G.; Kelly, J.
	1997	Interspecies sequence differences in the Mip protein from the genus Legionella: implications for function and evolutionary relatedness	Ratcliff, R.; Donnellan, S.; Lanser, J.; Manning, P.; Heuzenroeder, M.
	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.