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Preview	Issue Date	Title	Author(s)
	2011	Functional performance in young Australian children with achondroplasia	Ireland, P.; McGill, J.; Zankl, A.; Ware, R.; Pacey, V.; Ault, J.; Savarirayan, R.; Sillence, D.; Thompson, E.; Townshend, S.; Johnston, L.
	2011	Time demands of caring for children with cerebral palsy: what are the implications for maternal mental health?	Sawyer, M.; Bittman, M.; La Greca, A.; Crettenden, A.; Borojevic, N.; Russo, R.; Raghavendra, P.
	2011	Screening patients referred to a metabolic clinic for lysosomal storage disorders	Fuller, M.; Tucker, J.; Lang, D.; Dean, C.; Fietz, M.; Meikle, P.; Hopwood, J.
	2012	Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): A new autosomal dominant syndrome	Worthley, D.; Phillips, K.; Wayte, N.; Schrader, K.; Healey, S.; Kaurah, P.; Shulkes, A.; Grimpen, F.; Clouston, A.; Moore, D.; Cullen, D.; Ormonde, D.; Mounkley, D.; Wen, X.; Lindor, N.; Carniero, F.; Huntsman, D.; Chenevix-Trench, G.; Suthers, G.
	2012	Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing	Calvo, S.; Compton, A.; Hershman, S.; Lim, S.; Lieber, D.; Tucker, E.; Laskowski, A.; Garone, C.; Liu, S.; Jaffe, D.; Christodoulou, J.; Fletcher, J.; Bruno, D.; Goldblatt, J.; DiMauro, S.; Thorburn, D.; Mootha, V.
	2010	Differences in parental attitudes towards sleep and associations with sleep-wake patterns in Caucasian and Southeast Asian school-aged children in Australia	Biggs, S.; Pizzorno, V.; van den Heuvel, C.; Kennedy, J.; Martin, A.; Lushington, K.
	2011	De novo SCN1A mutations in migrating partial seizures of infancy	Carranza Rojo, D.; Hamiwka, L.; McMahon, J.; Dibbens, L.; Arsov, T.; Suls, A.; Stodberg, T.; Kelley, K.; Wirrell, E.; Appleton, B.; Mackay, M.; Freeman, J.; Yendle, S.; Berkovic, S.; Bienvenu, T.; De Jonghe, P.; Thorburn, D.; Mulley, J.; Mefford, H.; Scheffer, I.
	2010	Increased thrombophilic tendency in pediatric cystic fibrosis patients	Williams, V.; Griffiths, A.; Yap, Z.; Martin, J.; Smith, G.; Couper, R.; Revesz, T.
	2010	Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families	Hynes, K.; Tarpey, P.; Dibbens, L.; Bayly, M.; Berkovic, S.; Smith, R.; Al Raisi, Z.; Turner, S.; Brown, N.; Desai, T.; Haan, E.; Turner, G.; Christodoulou, J.; Leonard, H.; Gill, D.; Stratton, M.; Gecz, J.; Scheffer, I.
	2013	Umbilical cord blood testosterone and childhood internalizing and externalizing behavior: a prospective study	Robinson, M.; Whitehouse, A.; Jacoby, P.; Mattes, E.; Sawyer, M.; Keelan, J.; Hickey, M.; Schooling, C.M.