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Preview	Issue Date	Title	Author(s)
	2002	Recombinant Human Bone Morphogenetic Protein-2 for Treatment of Open Tibial Fractures	Csimma, C.; Genant, H.; Valentin-Opran, A.; Amit, Y.; Arbel, R.; Aro, H.; Atar, D.; Bishay, M.; Borner, M.; Chiron, P.; Choong, P.; Cinats, J.; Courtenay, B.; Feibel, R.; Geulette, B.; Gravel, C.; Haas, N.; Raschke, M.; Hammacher, E.; van der Velde, D.; et al.
	2002	Repair of Groin Hernia With Synthetic Mesh: Meta-Analysis of Randomized Controlled Trials	Grant, A.; Go, P.; Fingerhut, A.; Kingsnorth, A.; Merello, J.; O'Dwyer, P.; Payne, J.; McCormack, K.; Ross, S.; Scott, N.; Vale, L.; Aitola, P.; Anderberg, B.; Barkun, J.; Barth Jnr, R.; Bay-Nielsen, M.; Bittner, R.; Bringman, S.; Callesen, T.; Castoro, C.; et al.
	2002	Considerations for the safe prescribing and use of COX-2-specific inhibitors	Barraclough, D.; Bertouch, J.; Brooks, P.; Brown, M.; Cleland, L.; Clemens, L.; Crowley, S.; Day, R.; DeJager, J.; Edmonds, J.; Fletcher, P.; Franks, G.; Harris, D.; Horowitz, J.; Johnston, M.; Kerr, S.; Littlejohn, G.; MacDonald, G.; McColl, G.; Sambrook, P.; et al.
	2002	The reliability of immunohistochemistry as a prescreening method for the diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC) - Results of an international collaborative study	Muller, W.; Burgart, L.; Krause-Paulus, R.; Thibodeau, S.; Almeida, M.; Edmonston, T.; Boland, C.; Sutter, C.; Jass, J.; Lindblom, A.; Lubinski, J.; MacDermot, K.; Sanders, D.; Morreau, H.; Muller, A.; Oliani, C.; Orntoft, T.; Ponz De Leon, M.; Rosty, C.; Rodriguez-Bigas, M.; et al.
	2002	Laparoscopic versus open groin hernia repair: meta-analysis of randomised trials based on individual patient data	Fingerhut, A.; Go, P.; Grant, A.; Kingsnorth, A.; Merello, J.; O'Dwyer, P.; Payne, J.; McCormack, K.; Ross, S.; Scott, N.; Vale, L.; Aitola, P.; Anderberg, B.; Arvidsson, D.; Barkun, J.; Barth Jnr, R.; Bay-Nielsen, M.; Beets, G.; Bittner, R.; Bringman, S.; et al.
	2002	ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation	Bienvenu, T.; Poirier, K.; Friocourt, G.; Bahi, N.; Beaumont, D.; Fauchereau, F.; Jeema, L.; Zemni, R.; Vinet, M.; Francis, F.; Couvert, P.; Gomot, M.; Moraine, C.; van Bokhoven, H.; Kalscheuer, V.; Frints, S.; Gecz, J.; Ohzaki, K.; Chaabouni, H.; Fryns, J.; et al.
	2002	Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome	Lower, K.; Turner, G.; Kerr, B.; Mathews, K.; Shaw, M.; Gedeon, A.; Schelley, S.; Hoyme, H.; White, S.; Delatycki, M.; Lampe, A.; Clayton-Smith, J.; Stewart, H.; van Ravenswaay, C.; de Vries, B.; Cox, B.; Grompe, M.; Ross, S.; Thomas, P.; Mulley, J.; et al.