1. Adelaide Research & Scholarship

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Results 1061-1065 of 1065 (Search time: 0.006 seconds).
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PreviewIssue DateTitleAuthor(s)
2010A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32Hattersley, K.; Laurie, K.; Liebelt, J.; Gecz, J.; Durkin, S.; Craig, J.; Burden, K.
2019A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delayMucha, B.E.; Banka, S.; Ajeawung, N.F.; Molidperee, S.; Chen, G.G.; Koenig, M.K.; Adejumo, R.B.; Till, M.; Harbord, M.; Perrier, R.; Lemyre, E.; Boucher, R.M.; Skotko, B.G.; Waxler, J.L.; Thomas, M.A.; Hodge, J.C.; Gecz, J.; Nicholl, J.; McGregor, L.; Linden, T.; et al.
2024Exploring preconception health in adolescents and young adults: Identifying risk factors and interventions to prevent adverse maternal, perinatal, and child health outcomes-A scoping reviewPadhani, Z.A.; Rahim, K.A.; Tessema, G.A.; Avery, J.C.; Damabi, N.M.; Castleton, P.; Salam, R.A.; Meherali, S.; Lassi, Z.S.
2024The geographic distribution of invasive meningococcal disease and carriage: A spatial analysisMilazzo, A.; McMillan, M.; Giles, L.; Page, K.; Flood, L.; Marshall, H.
2023Prevalence, years lived with disability, and trends in anaemia burden by severity and cause, 1990-2021: findings from the Global Burden of Disease Study 2021Gardner, W.M.; Razo, C.; McHugh, T.A.; Hagins, H.; Vilchis-Tella, V.M.; Hennessy, C.; Taylor, H.J.; Perumal, N.; Fuller, K.; Cercy, K.M.; Zoeckler, L.Z.; Chen, C.S.; Lim, S.S.; Aali, A.; Abate, K.H.; Abd-Elsalam, S.; Abdurehman, A.M.; Abebe, G.; Abidi, H.; Aboagye, R.G.; et al.

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