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Preview	Issue Date	Title	Author(s)
	2003	Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation	Burdon, K.; McKay, J.; Sale, M.; Russell-Eggitt, I.; Mackey, D.; Wirth, G.; Elder, J.; Nicoll, A.; Clarke, M.; FitzGerald, L.; Stankovich, J.; Shaw, M.; Sharma, S.; Gajovic, S.; Gruss, P.; Ross, S.; Thomas, P.; Voss, A.; Thomas, T.; Gecz, J.; et al.
	2000	Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells	Ried, K.; Finnis, M.; Hobson, L.; Mangelsdorf, M.; Dayan, S.; Nancarrow, J.; Woollatt, E.; Kremmidiotis, G.; Gardner, A.; Venter, D.; Baker, E.; Richards, R.
	2007	Protein and gene expression analysis of Phf6, the gene mutated in the Borjeson-Forssman-Lehmann Syndrome of intellectual disability and obesity	Voss, A.; Gamble, R.; Collin, C.; Shoubridge, C.; Corbett, M.; Gecz, J.; Thomas, T.
	2000	Cloning of leptin cDNA and assignment to the long arm of chromosome 5 in the marsupial Sminthopsis crassicaudata	Hope, P.; Webb, G.; Lok, S.; Hope, R.; Turnbull, H.; Jelmberg, A.; Wittert, G.
	2004	Chorionic gonadotrophin b subunit mRNA but not luteinising hormone b subunit mRNA is expressed in the pituitary of the common marmoset (Callithrix jacchus)	Muller, T.; Simoni, M.; Pekel, E.; Luetjens, C.; Chandolia, R.; Amato, F.; Norman, R.; Gromoll, J.
	2001	Isolation, tissue distribution, and chromosomal localization of a novel testis-specific human four-transmembrane gene related to CD20 and FcRI-b	Hulett, M.; Pagler, E.; Hornby, J.; Hogarth, P.; Eyre, H.; Baker, E.; Crawford, J.; Sutherland, G.; Ohms, S.; Parish, C.