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Preview	Issue Date	Title	Author(s)
	1997	Genomic structure and complete nucleotide sequence of the Batten Disease Gene, CLN3	Mitchison, H.; Munroe, P.; O'Rawe, A.; Taschner, P.; De Vos, N.; Kremmidiotis, G.; Lensink, I.; Munk, A.; D'Arigo, K.; Anderson, J.; Lerner, T.; Moyzis, R.; Callen, D.; Breuning, M.; Doggett, N.; Gardiner, R.; Mole, S.
	1995	Mechanisms of small ring formation suggested by the molecular characterization of 2 small accessory ring chromosomes derived from chromosome 4	Fang, Y.; Eyre, H.; Bohlander, S.; Estop, A.; McPherson, E.; Trager, T.; Riess, O.; Callen, D.
	1996	Long-term in vitro correction of alpha-L-iduronidase deficiency (Hurler syndrome) in human bone marrow	Fairbairn, L.; Lashford, L.; Spooncer, E.; McDermott, R.; Lebens, G.; Arrand, J.; Arrand, J.; Bellantuono, I.; Holt, R.; Hatton, C.; Cooper, A.; Besley, G.; Wraith, J.; Anson, D.; Hopwood, J.; Dexter, T.
	1996	Identification, expression, and biochemical characterization of N-acetylgalactosamine-4-sulfatase mutations and relationship with clinical phenotype in MPS-VI patients	Litjens, T.; Brooks, D.; Peters, C.; Gibson, G.; Hopwood, J.
	1995	Luteinizing hormone/chorionic gonadotropin bioactivity in the common marmoset (Callithrix jacchus) is due to a chorionic gonadotropin molecule with a structure intermediate between human chorionic gonadotropin and human luteinizing hormone.	Simula, A.; Amato, F.; Faast, R.; Lopata, A.; Berka, J.; Norman, R.
	2000	FMR3 is a novel gene associated with FRAXE CpG island and transcriptionally silent in FRAXE full mutations	Gecz, J.
	2004	Nxf and Fbxo33: novel seizure-responsive genes in mice	Flood, W.; Moyer, R.; Tsykin, A.; Sutherland, G.; Koblar, S.
	1995	The brn-2 gene regulates the melanocytic phenotype and tumorigenic potential of human melanoma cells	Angus, J.; Thompson, F.; Murphy, K.; Baker, E.; Sutherland, G.; Parsons, P.; Sturm, R.
	1999	Testisin, a new human serine proteinase expressed by premeiotic testicular germ cells and lost in testicular germ cell tumors	Hooper, J.; Nicol, D.; Dickinson, J.; Eyre, H.; Scarman, A.; Normyle, J.; Stuttgen, M.; Douglas, M.; Loveland, K.; Sutherland, G.; Antalis, T.
	2008	Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoform	Sharma, S.; Burdon, K.; Dave, A.; Jamieson, R.; Yaron, Y.; Billson, F.; van Maldergem, L.; Lorenz, B.; Gecz, J.; Craig, J.