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Preview	Issue Date	Title	Author(s)
	2000	Universal periconceptional folate supplementation: chasing a dream?	Chan, A.; Haan, E.
	2009	Upper limb orthoses and assistive technology utilization in children with hemiplegic cerebral palsy recruited from a population register	Russo, R.; Atkins, R.; Haan, E.; Crotty, M.
	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.
	1998	What constitutes cerebral palsy?	Badawi, N.; Watson, L.; Petterson, B.; Blair, E.; Slee, J.; Haan, E.; Stanley, F.
	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.
	1999	X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisation	Woffendin, H.; Jakins, T.; Jouet, M.; Stewart, H.; Landy, S.; Haan, E.; Harris, A.; Donnai, D.; Read, A.; Kenwrick, S.
	2003	X-linked myotubular myopathy in a family with three adult survivors	Yu, S.; Manson, J.; White, S.; Bourne, A.; Waddy, H.; Davis, M.; Haan, E.
	2013	Yunis-Varón Syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatase	Campeau, P.; Lenk, G.; Lu, J.; Bae, Y.; Burrage, L.; Turnpenny, P.; Corona-Rivera, J.; Morandi, L.; Mora, M.; Reutter, H.; Vulto-van Silfhout, A.; Faivre, L.; Haan, E.; Gibbs, R.; Meisler, M.; Lee, B.
	2017	YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction	Gabriele, M.; Vulto-van Silfhout, A.; Germain, P.; Vitriolo, A.; Kumar, R.; Douglas, E.; Haan, E.; Kosaki, K.; Takenouchi, T.; Rauch, A.; Steindl, K.; Frengen, E.; Misceo, D.; Pedurupillay, C.; Stromme, P.; Rosenfeld, J.; Shao, Y.; Craigen, W.; Schaaf, C.; Rodriguez-Buritica, D.; et al.
	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 135 to 144 of 144 < previous