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Preview	Issue Date	Title	Author(s)
	1996	Gene localisation for Wilson-Turner syndrome (WTS:MIM 309585)	Gedeon, A.; Turner, G.; Mulley, J.
	1996	A novel mutation in Exon 6 (F236S) of the proteolipid protein gene is associated with spastic paraplegia	Donnelly, A.; Colley, A.; Crimmins, D.; Mulley, J.
	1996	Gene localisation for Sutherland-Haan syndrome (SHS:MIM 309470)	Gedeon, A.; Haan, E.; Mulley, J.
	1996	Refinement of the background genetic map of Xq26-q27 and gene localisation for Borjeson-Forssman-Lehmann syndrome	Gedeon, A.; Kozman, H.; Robinson, H.; Pilia, G.; Schlessinger, D.; Turner, G.; Mulley, J.
	1996	Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation	Gedeon, A.; Glass, I.; Connor, J.; Mulley, J.
	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.
	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.
	1999	Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardation	Gecz, J.; Barnett, S.; Liu, J.; Hollway, G.; Donnelly, A.; Eyre, H.; Eshkevari, H.; Baltazar, R.; Grunn, A.; Nagaraja, R.; Gilliam, C.; Peltonen, L.; Sutherland, G.; Baron, M.; Mulley, J.