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Preview	Issue Date	Title	Author(s)
	2008	Folate awareness and the prevalence of neural tube defects in South Australia, 1966-2007	Chan, A.; van Essen, P.; Scott, H.; Haan, E.; Sage, L.; Scott, J.; Gill, T.; Nguyen, A.
	2007	Upper-limb botulinum toxin A injection and occupational therapy in children with hemiplegic cerebral palsy identified from a population register: A single-blind, randomized, controlled trial	Russo, R.; Crotty, M.; Miller, M.; Murchland, S.; Flett, P.; Haan, E.
	1995	Maternal serum screening and prenatal diagnosis for birth defects	Suthers, G.; Haan, E.
	2008	Combining first and second trimester markers for Down syndrome screening: Think twice	Cocciolone, R.; Brameld, K.; OLeary, P.; Haan, E.; Muller, P.; Shand, K.
	1998	Effect of Parity, Gravidity, Previous Miscarriage, and Age On Risk of Downs-Syndrome - Population Based Study	Chan, A.; McCaul, K.; Keane, R.; Haan, E.
	1998	A population-based study of abdominal wall defects in South Australia and Western Australia	Byron-Scott, R.; Haan, E.; Chan, A.; Bower, C.; Scott, H.; Clark, K.
	1999	Origins of accessory small ring marker chromosomes derived from chromosome 1	Callen, D.; Eyre, H.; Fang, Y.; Guan, X.; Veleba, A.; Martin, N.; McGill, J.; Haan, E.
	1997	A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome	Muenke, M.; Gripp, K.; McDonald-McGinn, D.; Gaudenz, K.; Whitaker, L.; Bartlett, S.; Markowitz, R.; Robin, N.; Nwokoro, N.; Mulvihill, J.; Losken, H.; Mulliken, J.; Guttmacher, A.; Wilroy, R.; Clarke, L.; Hollway, G.; Ades, L.; Haan, E.; Mulley, J.; Cohen, M.; et al.
	2000	New mutations in MID1 provide support for loss of function as the cause of X-linked Optiz syndrome	Cox, T.; Allen, L.; Cox, L.; Hopwood, B.; Goodwin, B.; Haan, E.; Suthers, G.
	2000	Intention to undergo prophylactic bilateral mastectomy in women at increased risk of developing hereditary breast cancer	Meiser, B.; Butow, P.; Friedlander, M.; Schnieden, V.; Gattas, M.; Kirk, J.; Suthers, G.; Haan, E.; Tucker, K.