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Preview	Issue Date	Title	Author(s)
	2013	Single-nucleotide polymorphism associations with preterm delivery: a case-control replication study and meta-analysis	O'Callaghan, M.; MacLennan, A.; McMichael, G.; Haan, E.; 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.
	2005	The Hunter-McAlpine syndrome results from duplication 5q35-qter	Hunter, A.; DuPont, B.; McLaughlin, M.; Hinton, L.; Baker, E.; Ades, L.; Haan, E.; Schwartz, C.
	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.
	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 20 to 26 of 26 < previous