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Results 11-20 of 27 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2016HUWE1 mutations in Juberg-Marsidi and Brooks syndromes: the results of an X-chromosome exome sequencing studyFriez, M.; Brooks, S.; Stevenson, R.; Field, M.; Basehore, M.; Adès, L.; Sebold, C.; Mcgee, S.; Saxon, S.; Skinner, C.; Craig, M.; Murray, L.; Simensen, R.; Yap, Y.; Shaw, M.; Gardner, A.; Corbett, M.; Kumar, R.; Bosshard, M.; Van Loon, B.; et al.
2016A longitudinal study of adjustment disorder after trauma exposureO'Donnell, M.L.; Alkemade, N.; Creamer, M.; McFarlane, A.C.; Silove, D.; Bryant, R.A.; Felmingham, K.; Steel, Z.; Forbes, D.
2016Visual cues of object properties differentially affect anticipatory planning of digit forces and placementLee-Miller, T.; Marneweck, M.; Santello, M.; Gordon, A.; Buckingham, G.
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.
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.
2016The role of surgery in the management of phantosmiaMorrissey, D.; Pratap, U.; Brown, C.; Wormald, P.
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.
2016Natural history and long-term impact of dental fluorosis: a prospective cohort studyDo, L.; Ha, D.; Spencer, A.

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