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Preview	Issue Date	Title	Author(s)
	2014	The impact of Aboriginal status, cigarette smoking and smoking cessation on perinatal outcomes in South Australia	Hodyl, N.; Grzeskowiak, L.; Stark, M.; Scheil, W.; Clifton, V.
	2014	Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing	Buchanan, D.; Tan, Y.; Walsh, M.; Clendenning, M.; Metcalf, A.; Ferguson, K.; Arnold, S.; Thompson, B.; Lose, F.; Parsons, M.; Walters, R.; Pearson, S.; Cummings, M.; Oehler, M.; Blomfield, P.; Quinn, M.; Kirk, J.; Stewart, C.; Obermair, A.; Young, J.; et al.
	2014	Genetics of epilepsy: the testimony of twins in the molecular era	Vadlamudi, L.; Milne, R.; Lawrence, K.; Heron, S.; Eckhaus, J.; Keay, D.; Connellan, M.; Torn-Broers, Y.; Howell, R.; Mulley, J.; Scheffer, I.; Dibbens, L.; Hopper, J.; Berkovic, S.
	2014	Preconception dietary patterns in human pregnancies are associated with preterm delivery	Grieger, J.; Grzeskowiak, L.; Clifton, V.
	2014	Randomized controlled trial of maternal omega-3 long-chain PUFA supplementation during pregnancy and early childhood development of attention, working memory, and inhibitory control	Gould, J.; Makrides, M.; Colombo, J.; Smithers, L.
	2012	Neonatal outcomes after late-gestation exposure to selective serotonin reuptake inhibitors	Grzeskowiak, L.; Gilbert, A.; Morrison, J.
	2015	Incidence of curable sexually transmissible infections among adolescents and young adults in remote Australian Aboriginal communities: analysis of longitudinal clinical service data	Silver, B.; Guy, R.; Wand, H.; Ward, J.; Rumbold, A.; Fairley, C.; Donovan, B.; Maher, L.; Dyda, A.; Garton, L.; Hengel, B.; Knox, J.; McGregor, S.; Taylor-Thomson, D.; Kaldor, J.
	2015	Brain structural and microstructural alterations associated with cerebral palsy and motor impairments in adolescents born extremely preterm and/or extremely low birthweight	Kelly, C.E.; Chan, L.; Burnett, A.C.; Lee, K.J.; Connelly, A.; Anderson, P.J.; Doyle, L.W.; Cheong, J.L.Y.; Thompson, D.K.
	2016	X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes	Hu, H.; Haas, S.; Chelly, J.; Van Esch, H.; Raynaud, M.; De Brouwer, A.; Weinert, S.; Froyen, G.; Frints, S.; Laumonnier, F.; Zemojtel, T.; Love, M.; Richard, H.; Emde, A.; Bienek, M.; Jensen, C.; Hambrock, M.; Fischer, U.; Langnick, C.; Feldkamp, M.; et al.
	2016	Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID	van Bon, B.W.M.; Coe, B.P.; Bernier, R.; Green, C.; Gerdts, J.; Witherspoon, K.; Kleefstra, T.; Willemsen, M.H.; Kumar, R.; Bosco, P.; Fichera, M.; Li, D.; Amaral, D.; Cristofoli, F.; Peeters, H.; Haan, E.; Romano, C.; Mefford, H.C.; Scheffer, I.; Gecz, J.; et al.