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Results 11-20 of 34 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2016Characterizing and predicting trajectories of disordered eating over adolescenceFairweather-Schmidt, A.K.; Wade, T.D.
2016Residential location and kidney transplant outcomes in indigenous compared with nonindigenous AustraliansBarraclough, K.; Grace, B.; Lawton, P.; McDonald, S.
2016The psycho-social impact of malocclusions and treatment expectations of adolescent orthodontic patientsTwigge, E.; Roberts, R.; Jamieson, L.; Dreyer, C.; Sampson, W.
2016The long-term psychiatric sequelae of severe injury: a 6-year follow-up studyO'Donnell, M.; Alkemade, N.; Creamer, M.; McFarlane, A.; Silove, D.; Bryant, R.; Forbes, D.
2016Evidence for central hypercortisolism and elevated blood pressure in adolescent offspring of mothers with pre-eclampsiaHenley, D.; Brown, S.; Pennell, C.; Lye, S.; Torpy, D.
2016Optimal timing of delivery among low-risk women with prior caesarean section: a secondary analysis of the WHO multicountry survey on maternal and newborn healthGanchimeg, T.; Nagata, C.; Vogel, J.; Morisaki, N.; Pileggi-Castro, C.; Ortiz-Panozo, E.; Jayaratne, K.; Mittal, S.; Ota, E.; Souza, J.; Mori, R.; Crowther, C.; WHO Multicountry Survey on Maternal and Newborn Health Research Network,; Räisänen, S.
2016Sex determination from fingerprint ridge density and white line counts in FilipinosTaduran, R.; Tadeo, A.; Escalona, N.; Townsend, G.
2016X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesHu, 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.
2016Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and IDvan 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.
2016Xp11.2 microduplications including IQSEC2, TSPYL2 and KDM5C genes in patients with neurodevelopmental disordersMoey, C.; Hinze, S.; Brueton, L.; Morton, J.; McMullan, D.; Kamien, B.; Barnett, C.; Brunetti-Pierri, N.; Nicholl, J.; Gecz, J.; Shoubridge, C.

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