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Showing results 38 to 46 of 46 < previous

Preview	Issue Date	Title	Author(s)
	2008	The antenatal causes of cerebral palsy - Genetic and viral associations	Gibson, C.; MacLennan, A.; Goldwater, P.; Dekker, G.
	2006	The association between inherited cytokine polymorphisms and cerebral palsy	Gibson, C.; MacLennan, A.; Goldwater, P.; Haan, E.; Priest, K.; Dekker, G.; Hague, W.; Morton, M.
	2011	The Australian cerebral palsy research study - Protocol for a national collaborative study investigating genomic and clinical associations with cerebral palsy	O'Callaghan, M.; MacLennan, A.; Gibson, C.; McMichael, G.; Haan, E.; Broadbent, J.; Priest, K.; Goldwater, P.; Dekker, G.
	2009	The genomic basis of cerebral palsy: A HuGE systematic literature review	O'Callaghan, M.; MacLennan, A.; Haan, E.; Dekker, G.
	1995	The origins of cerebral palsy - A consensus statement	MacLennan, A.; Stanley, F.; Blair, E.; Rice, G.; Stone, P.; Robinson, J.; Henderson-Smart, D.; Yu, V.; Harbord, M.; Stern, L.; Chambers, H.; Furness, M.; Hayward, T.; Eckert, K.; Boundy, C.; Merrett, S.; Kenny, M.
	2005	The prevalence of inherited thrombophilias in a Caucasian Australian population	Gibson, C.; MacLennan, A.; Rudzki, Z.; Hague, W.; Haan, E.; Sharpe, P.; Priest, K.; Chan, A.; Dekker, G.; Khong, T.
	2005	Who will deliver our grandchildren? Implications of cerebral palsy litigation	MacLennan, A.; Nelson, K.; Hankins, G.; Speer, M.
	2002	Who will deliver the next generation of Australians?	MacLennan, A.; Spencer, M.
	2013	ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity	Hirata, H.; McMichael, G.; Haan, E.; MacLennan, A.; Yap, T.; Nguyen, L.; Shaw, M.; Gecz, J.

Showing results 38 to 46 of 46 < previous