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Preview	Issue Date	Title	Author(s)
	2002	The risk of mortality or cerebral palsy in twins: A collaborative population-based study	Scher, A.; Petterson, B.; Blair, E.; Ellenberg, J.; Grether, J.; Haan, E.; Reddihough, D.; Yeargin-Allsopp, M.; Nelson, K.
	1996	Characterisation of four novel fibrillin-1 mutations in the Marfan syndrome	Ades, L.; Haan, E.; Colley, A.; Richards, R.
	2015	Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy	McMichael, G.; Bainbridge, M.; Haan, E.; Corbett, M.; Gardner, A.; Thompson, S.; Van Bon, B.; Van Eyk, C.; Broadbent, J.; Reynolds, C.; O'Callaghan, M.; Nguyen, L.; Adelson, D.; Russo, R.; Jhangiani, S.; Doddapaneni, H.; Muzny, D.; Gibbs, R.; Gecz, J.; MacLennan, A.
	2002	Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies	Baker, E.; Hinton, L.; Callen, D.; Altree, M.; Dobbie, A.; Eyre, H.; Sutherland, G.; Thompson, E.; Thompson, P.; Woollatt, E.; Haan, E.
	2013	RPGR mutations might cause reduced orientation of respiratory cilia	Bukowy-Blerytto, Z.; Zletkiewicz, E.; Loges, N.; Wittmer, M.; Geremek, M.; Olbrich, H.; Filegauf, M.; Voelkel, K.; Rutkiewicz, E.; Rutland, J.; Morgan, L.; Pogorzelski, A.; Martin, A.; Haan, E.; Berger, W.; Omran, H.; Witt, M.
	2013	Epilepsy with cognitive deficit and autism spectrum disorders: Prospective diagnosis by array CGH	Nicholl, J.; Waters, W.; Suwalski, S.; Brown, S.; Hull, Y.; Harbord, M.; Entwistle, J.; Thompson, S.; Clark, D.; Pridmore, C.; Haan, E.; Barnett, C.; McGregor, L.; Liebelt, J.; Thompson, E.; Friend, K.; Bain, S.; Yu, S.; Mulley, J.
	2006	FBN1, TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisited	Ades, L.; Sullivan, K.; Biggin, A.; Haan, E.; Brett, M.; Holman, K.; Dixon, J.; Robertson, S.; Holmes, A.; Rogers, J.; Bennetts, B.
	2003	PEHO and PEHO-like syndromes: Report of five Australian cases	Field, M.; Grattan-Smith, P.; Piper, S.; Thompson, E.; Haan, E.; Edwards, M.; James, S.; Wilkinson, I.; Ades, L.
	1995	Prenatal exposure to phenytoin, facial development and a possible role for vitamin K	Howe, A.; Lipson, A.; Sheffield, L.; Haan, E.; Halliday, J.; Jensen, F.; David, D.; Webster, W.
	1995	Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndrome	Ades, L.; Morris, L.; Power, R.; Wilson, M.; Haan, E.; Bateman, J.; Milewicz, D.; Sillence, D.